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Artisan Vapor & CBD was cited for selling electronic nicotine delivery system (ENDS) products without required premarket authorization. The company's vaping and nicotine products fell under FDA jurisdiction as tobacco products containing nicotine from any source, which became subject to FDA regulation following the 2022 Consolidated Appropriations Act that expanded the definition of regulated tobacco products. The Center for Tobacco Products determined that these products were being distributed in the United States in violation of section 910 of the Federal Food, Drug, and Cosmetic Act, which requires new tobacco products to obtain premarket authorization before legal marketing.