Haviv Arazi
Fliq Vapor LLC
502 Gravesend Neck Rd.
Brooklyn , NY 11558
United States
support@fliqvapor.com
info@fliqvapor.comFEI 3015631064Issued Mar 25, 2022Center for Tobacco Products
Source: FDA, published letter. FDA published this warning letter; View Letter opens FDA's copy. To check it, open FDA's record for this establishment, listed under FEI 3015631064.
Violations1
Issue DateMar 25, 2022
Product TypeTobacco
StatusOpen
Letter Details
Firm
Fliq Vapor LLC
Location
Haviv Arazi
Fliq Vapor LLC
502 Gravesend Neck Rd.
Brooklyn , NY 11558
United States
support@fliqvapor.com
info@fliqvapor.com
FEI Number
3015631064
Country
United States
Issue Date
March 25, 2022
Issuing Office
Center for Tobacco Products
Product Type
Tobacco
Status
Open
Summary
Fliq Vapor LLC was warned for manufacturing and distributing electronic nicotine delivery system (ENDS) products without required premarket authorization. The FDA determined that the company's ENDS products listed on their website constituted "new tobacco products" under the Family Smoking Prevention and Tobacco Control Act and required premarket approval orders under section 910 of the Federal Food, Drug, and Cosmetic Act to be legally marketed in the United States. The company failed to obtain the necessary marketing authorization before offering these products for sale or distribution to U.S. customers.