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Vapor Lounge, LLC was warned for manufacturing and distributing e-liquid tobacco products without required premarket authorization as mandated by the Family Smoking Prevention and Tobacco Control Act. The company's e-liquid products, which are electronic nicotine delivery systems deemed subject to FDA regulation since August 8, 2016, were found to be in violation of Federal Food, Drug, and Cosmetic Act requirements for "new tobacco products" that must obtain marketing authorization before commercial distribution. The FDA determined that Vapor Lounge was manufacturing and offering these products for sale in the United States without compliance with applicable tobacco product regulations.