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Shenzhen Quawins Technology Co., Ltd was cited for manufacturing and distributing electronic nicotine delivery system (ENDS) products in the United States without required premarket authorization under the Family Smoking Prevention and Tobacco Control Act. The company's ENDS products, offered for sale through their website, were deemed new tobacco products subject to FDA jurisdiction but lacked the mandatory marketing authorization orders required by section 910 of the Federal Food, Drug, and Cosmetic Act. As of the warning date in November 2022, these products remained in violation of FDA regulations governing tobacco product marketing and distribution.