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Shenzhen GreenSound High-Tech Co., LTD d/b/a Vaporlax was cited for manufacturing and distributing electronic nicotine delivery systems (ENDS) products through their website without required premarket authorization from the FDA. The company failed to comply with the Family Smoking Prevention and Tobacco Control Act by marketing these tobacco products without obtaining a marketing authorization order under section 910 of the Federal Food, Drug, and Cosmetic Act, which has been required for new tobacco products since August 8, 2016. The FDA determined that the ENDS products listed on vaporlax.com were being offered for sale or distribution to U.S. customers and therefore subject to FDA jurisdiction and premarket review requirements.