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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's vapor products, which contain nicotine from any source, are classified as tobacco products under FDA jurisdiction and must comply with Federal Food, Drug, and Cosmetic Act requirements, including obtaining marketing authorization for "new tobacco products" not commercially marketed before February 15, 2007. The FDA determined the company was distributing these unapproved tobacco products in violation of section 910(a) of the FD&C Act and related regulations.