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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
Boss Vapes Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
UIS Manufacturing, LLC d/b/a UIS Vapes Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
E-Cig Vape Lounge LLP Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
Shop Vapes Inc. Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
DFW Vapor Holdings Inc. d/b/a Vapor Lakes, Inc. Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
Advanced Nutriceuticals, LLC dba The Guyer Institute of Molecular Medicine Division of Pharmaceutical Quality Operations Division III Compounding Pharmacy/Adulterated Drug Products
Simply Vapour LLC dba Simply Vapour Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded
Global Sanitizers LLC Division of Pharmaceutical Quality Operations IV CGMP/Finished Pharmaceuticals/Adulterated
JD's Market Inc. Division of West Coast Imports Foreign Supplier Verification Program (FSVP)
Vape Hut Inc Center for Tobacco Products Family Smoking Prevention and Tobacco Control Act/Adulterated/Misbranded

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