EIN: 521512339
UEI: CKLTHNMJL8G4
Management decision deadline — for entities that funded this organization
The FAC accepted this audit on June 8, 2026. Under 2 CFR 200.521(d), a pass-through entity that provided federal funds to this organization for this audit period must issue a management decision on these findings by December 8, 2026 (111 days from today).
What is a management decision? →Finding 2023-001: Audit Delays Federal Agency: United States Department of Agriculture Federal Program: Foreign Market Development Cooperator Program (FMD) Assistance Listing Number: 10.600 Pass-through Entity, if Applicable: None Award Identification Number and Year: F23GXCHSHO, F23GXCHDES, F23GXWWDES, F23GXSTNDS, F22GXEVALU Criteria or Specific Requirement: As noted in 2 CFR §200.512 the audit report should be submitted nine months after the end of the audit period. Condition: There were delays in receiving certain audit requests. The delays resulted in a late filing of the Uniform Guidance audit. Cause: The late submission resulted from delays in the audit process. Effect: Timely year-end closure is important to avoid increased potential for fraud, misstatements, and failures to adhere to donor and other regulations. Effective filing of documents decreases the potential for non-compliance with donor requirements, questioned costs or findings. Questioned Costs: None identified. Context: The filing is due nine months after fiscal year-end. Identification as a Repeat Finding, if Applicable: This is not a repeat finding. Recommendation: We recommend that LHCA ensure that the Uniform Guidance report is filed on time. A timely year-end closure, and appropriate maintenance and filing of financial and compliance documents, will help ensure that the report can be filed on time.
Views of Responsible Officials and Planned Corrective Actions: LHCA acknowledges that the 2023 Uniform Guidance audit was submitted after the nine-month deadline required under 2 CFR §200.512. We take our compliance obligations seriously and are committed to timely submission going forward. LHCA acknowledges that, regardless of contributing factors, the responsibility for timely submission rests with the organization under 2 CFR 200.512. To ensure timely completion in future years, LHCA has implemented the following corrective actions: A dedicated audit liaison has been designated to coordinate all auditor requests and ensure document delivery within 72 hours of any request.Moving forward, LHCA will formally engage its audit firm no later than February 1st of each subsequent audit year, allowing sufficient time for fieldwork to be completed well in advance of the September 30th submission deadline. At engagement initiation, LHCA and its audit firm will establish a shared audit timeline with agreed milestone dates for fieldwork completion, draft report delivery, management response, and final FAC submission, with September 15th as the internal target submission date to provide a two-week buffer before the regulatory deadline. Financial records and grant documentation are now organized in a standardized Google Drive structure that allows immediate retrieval of any document requested during the audit process, reducing response time, and eliminating documentation delays as a source of audit timeline risk. LHCA is confident these measures will prevent recurrence and ensure timely submission of all future Uniform Guidance audits.
Finding 2023-002: Procurement Federal Agency: United States Department of Agriculture Federal Program: Foreign Market Development Cooperator Program (FMD) Assistance Listing Number: 10.600 Pass-through Entity, if Applicable: None Award Identification Number and Year: F23GXCHSHO, F23GXCHDES, F23GXWWDES, F23GXSTNDS, F22GXEVALU Criteria or Specific Requirement: In accordance with the Organization's policy and 2 CFR 200.320 "Procurement Methods", price or rate quotations must be obtained from an adequate number of qualified sources for purchases over the applicable threshold. The Organization's guidelines include requirements to conduct an appropriate form of competition every three years on all multi-year contracts that are governed by the contracting guidelines. Also per the policy, contracts for market representation are not required to be re-competed after the initial reward. Instead, the performance of market representation must be evaluated and documented by the Organization annually to ensure that the terms of the contract are being met in a satisfactory manner. Condition: We noted opportunities to strengthen procurement documentation. In one instance, the selection analysis was not dated or formally approved and did not clearly identify the contract to which it related. In another instance, while documentation indicated that a request for proposal (RFP) was issued, no additional evaluation documentation or award conclusion was retained. Additionally, we noted an instance in which a market representative, for which re-competition is not required after the initial award, engaged under the USDA Market Access Program (MAP) was utilized to provide logistics support services, with costs charged to the Foreign Market Development (FMD) program.Based on discussions with management, logistics coordination is included within the scope of the China market representative’s original MAP contract. As such, these services were considered ancillary to the representative’s role and exempt from separate procurement requirements. However, contemporaneous documentation did not clearly demonstrate the formal rationale supporting the use of a noncompetitive procurement method under the FMD program. Strengthening documentation in this area would improve transparency and support compliance with applicable Federal requirements. Cause: Controls over procurement documentation and periodic compliance review were not sufficiently formalized to ensure consistent alignment with Uniform Guidance requirements. Effect: There is a risk that the Organization will not perform proper evaluation of each element of cost to determine reasonableness. Questioned Costs: None noted. Context: Our audit procedures consisted of statistical sampling as well as substantive testwork over various samples of expenditures, and were deemed to be representative of the population for the fiscal year under audit. Identification as a Repeat Finding, if Applicable: This is not a repeat finding. Recommendation: We recommend the Organization strengthen its procurement documentation and compliance procedures to ensure alignment with 2 CFR Part 200, as well as other applicable program guidelines. Specifically, the Organization should: Ensure all selection analyses are dated, formally approved, and clearly reference the applicable contract. Retain complete procurement files, including RFP documentation, evaluation criteria, scoring or comparative analyses, and documented award determinations. Implement a standardized procurement checklist to promote consistent documentation of the procurement rationale, selection process, and price reasonableness. For services provided by market representatives that are outside the original scope or are separately identifiable, perform appropriate competitive procurement procedures or clearly document the justification for a noncompetitive approach. Strengthening these procedures would enhance transparency, improve audit defensibility, and reduce the risk of questioned costs.
Views of Responsible Officials and Planned Corrective Actions: LHCA acknowledges that in two instances procurement documentation was administratively incomplete. In both cases the underlying competitive process was sound, vendors were evaluated, the appropriate vendor was selected, and the executed contracts reflect those outcomes. No questioned costs were identified. In the first instance, a completed evaluation matrix existed with vendor scoring but did not include a formal notation confirming the award conclusion. LHCA operates in a fully electronic environment where wet signatures are not standard practice. Going forward, documentation systems are in place so that explicit award conclusion notation will be included in the vendor file to make the selection decision self-evident to any reviewer without requiring supplemental explanation.In the second instance, complete procurement documentation existed at the time of the audit but was not delivered to auditors in a timely manner due to staff turnover. This was a document retrieval issue, not a documentation gap. LHCA has addressed this by centralizing all procurement documentation in a shared Google Drive repository that is immediately accessible regardless of staff changes, and by designating a dedicated audit liaison responsible for maintaining and producing all procurement files on request. Going forward, LHCA will incorporate a conflict-of-interest representation clause into all contractor agreements, including the Meat Institute management agreement, effective with the next contract cycle. Annual execution of each contract will serve as the annual conflict of interest certification required under 2 CFR §200.318(c) and LHCA's contracting guidelines, eliminating the need for a separate certification process outside of Executive Board officers involved in procurement. Regarding the market representative relationships. LHCA's market representative relationships were competitively awarded at inception, and are maintained through annual performance evaluation consistent with MAP §1485.29(d)(5), which explicitly replaces periodic re-competition with annual performance evaluation for the life of the relationship. Where a market representative engaged under MAP takes on additional related work funded under other programs such as FMD, the regulatory framework supports an approach other than a new competitive RFP. MAP §1485.29(d)(5) establishes that market representative relationships are not subject to periodic re-competition by virtue of their specialized and relational nature. FMD §1484.35 requires documented price reasonableness but does not prescribe the specific mechanism. 2 CFR §200.320, which applies to both programs by incorporation, recognizes that noncompetitive procurement is appropriate where only one source is reasonably available. Taken together, these provisions support the conclusion that where an existing market representative is the only practicable source for incremental related work — by virtue of their established relationships, market knowledge, commodity expertise, and program continuity — a formal proposal-based review process satisfies the regulatory intent without requiring a competitive process that would produce no meaningful competition. LHCA therefore requires the market representative to submit a formal written proposal for any expanded scope, with deliverables, timelines, and line-item costs sufficient to support a documented price reasonableness analysis. A contract amendment is executed only upon a determination that the proposed scope and cost represent reasonable value. This satisfies the regulatory intent of MAP §1485.29(d)(5), FMD §1484.35, and 2 CFR §200.320 without requiring a competitive process contrary to program interests. LHCA will incorporate this procedure explicitly into its contracting guidelines to ensure consistent application and clear documentation of the policy basis going forward.
Finding 2023-003: Contribution Requirement Documentation Federal Agency: United States Department of Agriculture Federal Program: Foreign Market Development Cooperator Program (FMD) Assistance Listing Number: 10.600 Pass-through Entity, if Applicable: NoneAward Identification Number and Year: F23GXCHSHO, F23GXCHDES, F23GXWWDES, F23GXSTNDS, F22GXEVALU Criteria or Specific Requirement: The 2023 Foreign Market Development Cooperator Program approval letter requires a contribution level of 70% of project expenditures. This amount may include cash, goods, or services provided by U.S. entities in support of LHCA’s FMD program. All contributions must be documented and verifiable by audit. Condition: During the audit, we noted inconsistencies in the documentation supporting reported contributions. Although the Organization ultimately provided a schedule showing how the requirement was met, the underlying support for contributions met by Laboratory and other expenses was in some cases not clearly documented, and lacked a clear review and approval process. The Organization received prior USDA guidance indicating that certain research conducted by the Leather Research Laboratory may qualify as industry contributions if aligned with USDA export promotion activities. However, not all Laboratory activities are allowable under the program. To capture the Laboratory’s contribution, the Organization initially provided a schedule summarizing related revenue as contributions. While using revenue as a basis to estimate and allocate qualifying costs is conceptually reasonable, the approach of reporting revenue alone was not permissible under Uniform Guidance (2 CFR Part 200), as revenue does not represent allowable, verifiable expenditures. Management subsequently provided a listing of actual Laboratory expenses believed to qualify as contributions, illustrating that the required contribution amount was met. Cause: The condition resulted from the absence of a formalized contributions policy and internal control process governing the identification, documentation, and review of allowable contributions. While management relied on general USDA guidance regarding qualifying industry contributions, the Organization did not establish detailed procedures to distinguish allowable from unallowable activities, or to ensure contributions were supported by verifiable expense documentation in accordance with Uniform Guidance. In addition, roles and responsibilities for review and approval were not clearly defined, resulting in inconsistent tracking methodologies and the use of an impermissible revenue-based approach. Effect: Contributions reported to USDA may not meet Uniform Guidance requirements, resulting in noncompliance and potential disallowance. Questioned Costs: None noted, as the Organization ultimately has numerous sources of contributions that illustrate that it met it's requirement, despite the inconsistent tracking and reporting. Context: Our audit procedures consisted of statistical sampling as well as substantive testwork over various samples of expenditures, and were deemed to be representative of the population for the fiscal year under audit. Identification as a Repeat Finding, if Applicable: This is not a repeat finding.Recommendation: We recommend the Organization establish and implement a formal contributions policy and review process to ensure amounts reported comply with Uniform Guidance (2 CFR Part 200) and program requirements. The policy should clearly define allowable contributions activities, require that reported amounts be supported by verifiable and auditable expense documentation (rather than revenue), and outline procedures for consistent tracking of personnel time and other contributions. Management should also implement a documented review and approval process to ensure contributions are accurate, allowable, and properly supported prior to submission. The Organization should also consult with USDA to formally clarify acceptable documentation and reporting requirements for industry contributions associated with lab activities.
Views of Responsible Officials and Planned Corrective Actions: LHCA's methodology for qualifying laboratory and affiliated organization expenses as industry in-kind contribution was developed in direct consultation with FAS program officials in June 2023. As documented in LHCA's written summary of that meeting, transmitted to senior FAS program and operations officials including the FMD program officer and acknowledged without objection, FAS validated the eligibility of research, marketing, policy, and technical expenses funded through industry funds, focused on target markets, and connected to UES activities. LHCA was acting on direct FAS guidance, not making unsupported determinations, and that documentation is available for the auditor's review. The revenue figures that appeared in LHCA's contribution documentation served as an allocation methodology, a proportional basis for determining what share of multi-purpose expenses relates to export promotion, not as the contribution itself. The actual contribution claimed consisted of underlying expenses allocated using that methodology. LHCA acknowledges that this methodology was not clearly labeled in the documentation provided to auditors, and will revise its documentation format to clearly distinguish the allocation calculation from the contribution amount claimed, ensuring the two are not conflated in future reviews. LHCA will formalize its contribution tracking procedures with a written policy document that defines eligible activities consistent with FAS guidance, specifies the allocation methodology and its basis, and requires that all claimed contribution be supported by verifiable expense documentation consistent with the hierarchy established in FMD §1484.33(f) and the cost principles in 2 CFR Part 200 Subpart E. A documented review and approval process will be implemented to ensure contribution amounts are accurate, allowable, and properly supported prior to submission.
Management decision deadline — for entities that funded this organization
The FAC accepted this audit on March 29, 2022. Under 2 CFR 200.521(d), a pass-through entity that provided federal funds to this organization for this audit period must issue a management decision on these findings by September 29, 2022, which was (1420 days ago).
What is a management decision? →Finding 2020-001: Suspension and Debarment Information on the Federal Programs: All Criteria or Specific Requirement: Recipients of Federal funding must adhere to specific requirements on screening all potential vendors, suppliers, contractors, subrecipients, employees, fellows, etc. to ensure the Organization is not conducting business with excluded parties (as defined by the United States Government). This screening process must also be documented in writing. Condition: Although it is our understanding that the Organization screened contractors in following with their policy, we were unable to verify that this screening was performed during the year under audit, because documentation was not maintained until subsequent to completion of the 2019 audit. Cause: Although the Organization was screening contractors in accordance with policy, the screening was not documented during the year under audit, so screenings related to 2020 were documented after the date of purchase. Effect: Failure to screen potential vendors, suppliers, contractors, subrecipients, employees, fellows, etc. against the suspended and debarred list increases the possibility that federal funds may inadvertently be provided to parties deemed to be excluded by the United States Government. Questioned Costs: Undetermined Context: Our audit procedures consisted of statistical sampling as well as substantive testwork over various samples of expenditures, and were deemed to be representative of the population for the fiscal year under audit. We determined that the issue was systemic in nature. Identification as a Repeat Finding, if Applicable: This is a repeat finding (2019-001) Recommendation: We recommend that the screening of potential vendors and suppliers be completed (and documented) prior to entering into the transactions or making payments, and should be periodically revisited (and documentation updated) for ongoing relationships with parties.
Views of Responsible Officials and Planned Corrective Actions: Effective March 9, 2021, all searches of contractors are documented with a screen shot of the website search results. Effective January 1, 2022, this action occurs each time a contract is entered into or renewed
2019-001
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