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  1. Compliance Actions and Activities

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
Everything Vapor Aztec Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
Vapor Salon Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
Safe Chain Solutions, LLC Division of Pharmaceutical Quality Operations I Drug Product/Adulterated
Schwebel Baking Company Division of Human and Animal Food Operations East V CGMP/Manufacturing, Packing or Holding Human Food/Adulterated/Insanitary Conditions
Suprimo Imports Center for Drug Evaluation and Research | CDER Unapproved New Drugs/Misbranded
Chengdu KeCheng Fine Chemicals Co., Ltd. Center for Drug Evaluation and Research | CDER CGMP/Active Pharmaceutical Ingredient (API)/Adulterated
A Perfect Vape, LLC Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
MV Store, Inc. d/b/a myvaporstore Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
ECigMafia LLC Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
The Hand Media, Inc. d/b/a Vapor Shark Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded

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