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Artisan Vapor Company was warned for selling e-liquid tobacco products without required premarket authorization from the FDA. The company failed to comply with the Family Smoking Prevention and Tobacco Control Act by distributing nicotine-containing products that were not commercially marketed as of February 15, 2007, and therefore qualify as "new tobacco products" requiring an approved marketing authorization order. The FDA determined the products were adulterated and misbranded under federal law, as they lacked the necessary premarket review and approval required for legal distribution in the United States.