Key facts
| Company | M G R Produce LLC |
|---|---|
| FDA office | Office of Inspections and Investigations |
| Letter date | June 2, 2026 |
| Subject / product | Foreign Supplier Verification Program (FSVP) |
| CFR citations | FDA Warning Letter |
| Response due | 15 working days from receipt (standard FDA warning-letter requirement) |
| Reference / source ID | m-g-r-produce-llc-730040-06022026 |
Violations explained
FDA Warning Letter — Violations FDA cited at M G R Produce LLC
WARNING LETTER M G R Produce LLC MARCS-CMS 730040 — June 02, 2026 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: Via Express Delivery Product: Food & Beverages Recipient: Recipient Name Mosiel G. Rodriguez Recipient Title Owner M G R Produce LLC 2615 Airline Dr Houston , TX 77009-1119 United States mgrproducellc@gmail.com Issuing Office: Office of Inspections and Investigations United States June 2, 2026 WARNING LETTER Re: CMS # 730040 Dear Mr. Mosiel Rodriguez: On 04/28/2026, the Food and Drug Administration (FDA) conducted a Foreign Supplier Verification Program (FSVP) inspection of M G R PRODUCE LLC located at 2615 Airline Dr Houston, TX 77009-1119. This inspection was 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 inspection, we found that you are not in compliance with the requirements of 21 CFR part 1, subpart L for the foods you import. 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 acknowledge receipt of your response, dated 05/05/2026 in which you stated the corrective actions that will be implemented by MGR Produce LLC, over a (b)(4) -month timeline. The plan provides a breakdown of the actions that will be completed month by month, as well as ongoing commitments to your responsibilities as an FSVP Importer. Your corrective action plan covers actions for assessment and gap analysis, hazard analysis development, supplier evaluation and approval, implementation of verification activities, and the corrective actions and program finalization. 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 1.502(a). Specifically, you did not develop an FSVP for any of the foods you import, including each of the following foods: Scallions, Green Onions, imported from, (b)(4) , located in (b)(4) Jicama, imported from, (b)(4) , located in (b)(4) Jalapenos, imported from, (b)(4) , located in (b)(4) You import fresh produce that may be considered “covered produce” as defined in 21 CFR 112.3. If after review of the fresh produce that you import you determine that you are an importer of covered produce, you must have an FSVP that demonstrates that your supplier is producing the food in compliance with processes and procedures that provide at least the same level of public health protection as those required under section 419 of the FD&C Act (21 U.S.C. 350h) (regarding standards for produce safety) and the implementing regulations in the Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption (21 CFR part 112). 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 section 805 of the FD&C Act and the implementing regulation in 21 CFR part 1, subpart L. (b)(3)(A) As a responsible official of a facility that manufactures/processes, packs, or holds food for human or animal consumption in the United States, you are responsible for ensuring that your overall operation a
What happens next
M G R Produce LLC is expected to respond to FDA in writing, typically within 15 working days of the letter date, describing the specific corrective and preventive actions taken or planned for each violation cited. FDA reviews that response and any follow-up evidence, and can conduct a re-inspection to confirm the corrections were actually made. If FDA judges the response inadequate, or the underlying conditions serious enough, further action can follow, including product seizure, injunction, import alert, or civil penalties; many Warning Letters are resolved through corrective action alone. This page reflects the Warning Letter as issued and will not reflect any subsequent correction unless FDA publishes a follow-up record. FDA issues Warning Letters after an inspection or other review when it believes a firm has significantly violated FDA regulations; the letter itself is a notice, not a final adjudication.
M G R Produce LLC’s FDA history
Argus HQ has recorded 1 total FDA action tied to M G R Produce LLC: 1 warning letter, 0 recalls, 0 approval records, and 0 Form 483 inspection citations.
Full letter text
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Frequently asked questions
- Which FDA office issued the warning letter to M G R Produce LLC?
- Office of Inspections and Investigations issued the warning letter to M G R Produce LLC.
- What CFR citations does this warning letter reference?
- The letter cites: FDA Warning Letter.
- Is the FDA warning letter to M G R Produce LLC publicly available?
- Yes. The full verbatim letter is published at fda.gov: https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/m-g-r-produce-llc-730040-06022026.
- 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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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). FDA Cites M G R Produce LLC in June 2, 2026 Warning Letter — Foreign Supplier Verification Program (FSVP). Digital Empire LLC. Retrieved from https://argushq.ai/warning-letter/m-g-r-produce-730040-2026-06-02
"FDA Cites M G R Produce LLC in June 2, 2026 Warning Letter — Foreign Supplier Verification Program (FSVP)." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/warning-letter/m-g-r-produce-730040-2026-06-02.
Argus HQ Research. "FDA Cites M G R Produce LLC in June 2, 2026 Warning Letter — Foreign Supplier Verification Program (FSVP)." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/warning-letter/m-g-r-produce-730040-2026-06-02.
@misc{argushq_argushq_ai_warning_letter_m_g_r_produce_730040_2026_06_02_2026,
title = {FDA Cites M G R Produce LLC in June 2, 2026 Warning Letter — Foreign Supplier Verification Program (FSVP)},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire LLC},
url = {https://argushq.ai/warning-letter/m-g-r-produce-730040-2026-06-02},
note = {Accessed: July 13, 2026}
}Source: FDA.gov — Warning Letters ↗

