Prida Import & Export LLC — FDA Warning Letter, 2026-04-10: Foreign Supplier Verification Program (FSVP)
Letter issued · posted to fda.gov .
Subject as published: Foreign Supplier Verification Program (FSVP)
TL;DR
Here's the summary: The FDA issued a warning letter to Prida Import & Export LLC (CEO Daniel Moussa, Doral, FL) on April 10, 2026, following an FSVP inspection conducted March 13-19, 2026, citing violations of 21 CFR part 1, subpart L for four imported food products: Powder Milk La Campestre, Powder Milk La Campina, Cilantro Sauce, and Chocolate Cream Spread Candy. The agency found that Prida failed to develop, maintain, and follow a Foreign Supplier Verification Program (FSVP) as required by section 805 of the FD&C Act, and requested a written response within 15 working days detailing corrective actions and supporting documentation. The FDA warned that failure to comply may result in refusal of admission, detention without physical examination of imported foods, or further enforcement action.
Argus analysis
# FDA Warning Letter Analysis: Prida Import & Export LLC
**Company Background and Findings**
Prida Import & Export LLC, a food importer based in Doral, Florida, received a warning letter from the FDA's Office of Inspections and Investigations on April 10, 2026, following an inspection conducted March 13–19, 2026. The FDA found that the company failed to establish and maintain a Foreign Supplier Verification Program (FSVP) for four imported food products: Powder Milk La Campestre, Powder Milk La Campina, Cilantro Sauce, and Chocolate Cream Spread Candy. This marked the third FDA inspection of the facility, with prior inspections occurring in January 2021 and April 2022, suggesting a pattern of non-compliance.
**Regulatory Citations and Meaning**
The violations center on 21 CFR Part 1, Subpart L (the FSVP regulation) and Section 805 of the Federal Food, Drug, and Cosmetic Act. These provisions require food importers to develop, maintain, and follow written verification programs demonstrating that foreign suppliers meet U.S. food safety standards. The regulation mandates risk-based supplier assessments, on-site audits, and documentation before importation. Prida's failure to develop any FSVP constitutes a fundamental breach of importer responsibilities under federal law.
**Response Timeline and Industry Monitoring**
Prida has 15 working days from receipt to submit a written response addressing the violations, including documentation of corrective actions and copies of newly developed FSVPs. Compliance officers in the food import sector should monitor for potential detention without physical examination (DWPE) of Prida's shipments under Import Alert 99-41 and possible refusal of admission. Failure to adequately respond may result in enforcement action under Section 801(a)(3) of the FD&C Act.
Severity context
Low severity. Procedural or narrow scope; most peer companies resolve in the 15-business-day response window without structural change.
Regulatory background
FDA Warning Letters are administratively non-binding but signal that recurring non-compliance may escalate to injunction, seizure, import alert, or Application Integrity Policy invocation.
What peer compliance teams typically do next
Most compliance officers at peer companies use a Warning Letter against a named entity as a checklist for their own CAPA program. Common steps: pull the verbatim FDA letter; map each cited 21 CFR section against the team’s SOP library; confirm CAPA coverage; brief the QMR (Quality Management Review) on whether the cited subject matter is in scope for the next internal audit. The 15-business-day response window applies to the cited entity, not to peers — but a documented internal review against the cited subjects is what regulators expect to see if a peer is later inspected on the same topic.
Excerpt from the FDA Warning Letter (public domain, 17 USC §105)
WARNING LETTER Prida Import & Export LLC MARCS-CMS 726912 — April 10, 2026 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: Via Email & Via Express Delivery Product: Food & Beverages Recipient: Recipient Name Daniel Moussa Recipient Title CEO Prida Import & Export LLC 10219 NW 62nd St Ste 10 Doral , FL 33178-4657 United States daniel@pridaimport.com Issuing Office: Office of Inspections and Investigations United States April 10, 2026 WARNING LETTER RE: CMS# 726912 Dear Mr. Daniel Moussa: From March 13th to 19th, 2026, the Food and Drug Administration (FDA) conducted a Foreign Supplier Verification Program (FSVP) inspection of Prida Import & Export LLC, located at 10219 NW 62nd St Ste 10, Doral, FL 33178-4657. We also conducted inspections on January 11th – 27th, 2021 and April 27th, 2022. These inspections were conducted to determine compliance with the requirements of section 805 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 384a) and the implementing FSVP regulation in 21 CFR part 1, subpart L. The FSVP regulation requires that importers perform certain risk-based activities to verify that human and/or animal food they import into the United States has been produced in a manner that meets applicable U.S. food safety standards. You may find information relating to the FSVP regulation and your responsibilities to comply with the regulation through links in FDA’s FSVP web page at https://www.fda.gov/food/food-safety-modernization-act-fsma/fsma-final-rule-foreign-supplier-verification-programs-fsvp-importers-food-humans-and-animals. During the most recent inspection, we found that you are not in compliance with the requirements of 21 CFR part 1, subpart L for the following foods you import: Powder Milk La Campestre from (b)(4) in (b)(4) ; Powder Milk La Campina from (b)(4) in (b)(4) ; Cilantro Sauce from (b)(4) in (b)(4) ; and Chocolate Cream Spread Candy from (b)(4) in (b)(4) . Because of these significant violations, you are not in compliance with section 805 of the FD&C Act. At the conclusion of the inspection, our investigator provided you with a Form FDA 483a FSVP Observations. We have not received your response to the Form FDA 483a issued on March 19th, 2026. Your significant violations of the FSVP regulation are as follows: You did not develop, maintain, and follow an FSVP as required by section 805 of the FD&C Act and 21 CFR part 1.502(a). Specifically, you did not develop an FSVP for any of the foods you import, including each of the following foods: Powder Milk La Campestre, imported from (b)(4) , located in (b)(4) Powder Milk La Campina, imported from (b)(4) , located in (b)(4) Cilantro Sauce, imported from (b)(4) , located in (b)(4) Chocolate Cream Spread Candy, imported from (b)(4) , located in (b)(4) The above violations are not intended to be an all-inclusive list of violations of the FSVP requirements. It is your responsibility to ensure that you are in compliance with sec…
Excerpt only. The full verbatim Warning Letter is the source of truth — always read the original before regulatory decisions.
The verbatim FDA Warning Letter is the source of truth. Always read the original before acting on any analysis or summary on this page.
Read the full letter on fda.gov ↗Frequently asked questions
- Is the FDA warning letter to Prida Import & Export LLC publicly available?
- Yes. The full verbatim letter is published at fda.gov. Argus HQ links directly to the source: https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/prida-import-export-llc-726912-04102026.
- What does a "low" severity rating mean for this letter?
- Low severity. Procedural or narrow scope; most peer companies resolve in the 15-business-day response window without structural change.
- What is the regulatory background for a Warning Letter warning letter?
- FDA Warning Letters are administratively non-binding but signal that recurring non-compliance may escalate to injunction, seizure, import alert, or Application Integrity Policy invocation.
- What is the standard FDA response window for a warning letter?
- FDA warning letters typically require a written response within 15 working days of receipt, outlining the corrective and preventive actions the company will take.
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methodology
The analysis above is produced by Anthropic Claude Haiku 4.5 against the verbatim FDA Warning Letter excerpt and is brand-voice lint-checked before publish. The TL;DR is the same summary that ships in the customer email digest. Severity is auto-classified by Argus from the subject string and letter body using rules documented in lib/ingestion/fda-warning-letters.ts.
Argus HQ is informational only. Summaries and analyses are AI-generated and may contain errors, misclassifications, or omissions. Verify against the FDA source URL above. Argus HQ is not a law firm, accounting firm, or regulatory agency, and provides no legal, accounting, financial, medical, or regulatory advice.
Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder
Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
Argus HQ Research (2026). Prida Import & Export LLC — FDA Warning Letter, 2026-04-10: Foreign Supplier Verification Program (FSVP). Digital Empire Holdings LLC. Retrieved from https://argushq.ai/fda/warning-letter/fda-wl-prida-import-and-export-llc-2026-04-10-warning-letter
"Prida Import & Export LLC — FDA Warning Letter, 2026-04-10: Foreign Supplier Verification Program (FSVP)." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/fda/warning-letter/fda-wl-prida-import-and-export-llc-2026-04-10-warning-letter.
Argus HQ Research. "Prida Import & Export LLC — FDA Warning Letter, 2026-04-10: Foreign Supplier Verification Program (FSVP)." Digital Empire Holdings LLC. Accessed July 29, 2026. https://argushq.ai/fda/warning-letter/fda-wl-prida-import-and-export-llc-2026-04-10-warning-letter.
@misc{argushq_argushq_ai_fda_warning_letter_fda_wl_prida_import_and_export_llc_2026_04_10_warning_letter_2026,
title = {Prida Import & Export LLC — FDA Warning Letter, 2026-04-10: Foreign Supplier Verification Program (FSVP)},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire Holdings LLC},
url = {https://argushq.ai/fda/warning-letter/fda-wl-prida-import-and-export-llc-2026-04-10-warning-letter},
note = {Accessed: July 29, 2026}
}