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  1. Compliance Actions and Activities

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
Wise Guys Vapes Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
Madvapes Vape Shop Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
Kure CBD & Vape Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
Kure CBD & Vape Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
OSRX, Inc. Center for Drug Evaluation and Research (CDER) Compounding Pharmacy/Adulterated Drug Products
Tailstorm Health Inc. dba Medivant Health Center for Drug Evaluation and Research (CDER) Compounding Pharmacy/Adulterated Drug Products
everythingvapes.com Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
Excelvision Fareva Center for Drug Evaluation and Research (CDER) CGMP/Finished Pharmaceuticals/Adulterated
Mentha & Allied Products Private Ltd. Center for Drug Evaluation and Research (CDER) CGMP/Active Pharmaceutical Ingredient (API)/Adulterated
Ningbo Riway Industrial Co., Ltd. Center for Drug Evaluation and Research (CDER) CGMP/Finished Pharmaceuticals/Unapproved New Drug/Misbranded/Adulterated

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