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Shenzhen Airis Electronic Co. Ltd. was warned for manufacturing and distributing electronic nicotine delivery system (ENDS) products through its website without required premarket authorization. The FDA determined the company's vaping products fall under tobacco product jurisdiction because they contain nicotine from any source, and as "new tobacco products" not commercially marketed in the U.S. before February 15, 2007, they were required to obtain a premarket authorization order before being legally sold. The company failed to comply with Federal Food, Drug, and Cosmetic Act requirements applicable to tobacco products under FDA's Center for Tobacco Products.