Warning Letters
Learn about the types of warning letters on FDA's website.
- Matters described in FDA warning letters may have been subject to subsequent interaction between FDA and the letter recipient that may have changed the regulatory status of issues discussed in the letter.
- To obtain additional available information, contact FDA. Requests to FDA for agency records should be sent to: Food and Drug Administration Division of Freedom of Information (HFI-35), 5630 Fishers Lane, Rockville, MD 20857. Instructions for how to submit an FOI request can be found at How to Make a FOIA Request.
| Posted Date | Letter Issue Date | Company Name | Issuing Office | Subject | Response Letter | Closeout Letter | Excerpt |
|---|---|---|---|---|---|---|---|
| Sambrosa Care Inc. | Center for Drug Evaluation and Research | CDER | Finished Pharmaceuticals/Unapproved New Drug/Misbranded | |||||
| Martin Farm, Konrad Martin | Division of Human and Animal Food Operations East VI | New Animal Drug/Adulterated | |||||
| Marion Mullet Farm | Division of Human and Animal Food Operations East VI | New Animal Drug/Adulterated |
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| S & J International Enterprises Public Company Limited | Center for Drug Evaluation and Research | CDER | CGMP/Finished Pharmaceuticals/Adulterated | |||||
| Grace Supply Inc. | Division of Southwest Imports | Foreign Supplier Verification Program (FSVP) | |||||
| Mexpobaja Corporation | Division of West Coast Imports | Foreign Supplier Verification Program (FSVP) | |||||
| A True Move LLC | Division of Southwest Imports | Foreign Supplier Verification Program (FSVP) | |||||
| JJR Global Inc. | Division of Southwest Imports | Foreign Supplier Verification Program (FSVP) | |||||
| Mei Lan Thailand Co., Ltd. | Center for Drug Evaluation and Research | CDER | CGMP/Active Pharmaceutical Ingredient (API)/Adulterated/Refused Inspection | |||||
| Cavevi Naturals LLC | Division of Southwest Imports | Foreign Supplier Verification Program (FSVP) |