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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.