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DIY Vapor Supply LLC was cited for manufacturing and distributing e-liquid tobacco products without required premarket authorization orders as mandated by the Family Smoking Prevention and Tobacco Control Act. The FDA determined that the company's e-liquids, offered for sale through their website, qualified as newly deemed tobacco products subject to FDA jurisdiction under the Federal Food, Drug, and Cosmetic Act but lacked the legally required marketing authorization to remain in commerce. The violation centered on the company's failure to obtain premarket approval before marketing these products, which became subject to FDA regulation effective August 8, 2016.