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Dell Vapers, an e-liquid tobacco product manufacturer, was cited for manufacturing and distributing tobacco products without obtaining required premarket authorization under the Family Smoking Prevention and Tobacco Control Act. The company failed to comply with FDA regulations governing newly deemed tobacco products, specifically electronic nicotine delivery systems (e-liquids), which have been subject to FDA jurisdiction since August 8, 2016. As "new tobacco products" not commercially marketed before February 15, 2007, the e-liquids required marketing authorization orders under section 910 of the Federal Food, Drug, and Cosmetic Act before distribution in the United States.