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Artisan Vapor Company was cited for selling electronic nicotine delivery system (ENDS) products without the required premarket authorization orders mandated by the Family Smoking Prevention and Tobacco Control Act. The company failed to comply with FDA regulations requiring "new tobacco products" to obtain marketing authorization before being legally distributed in the United States, a requirement that applies to all nicotine-containing products regardless of nicotine source following 2022 legislation. The Center for Tobacco Products determined the company's ENDS products were unapproved tobacco products being distributed in violation of the Federal Food, Drug, and Cosmetic Act and its implementing regulations.