Loading…
EZPuff Vapor Labs was warned for offering electronic nicotine delivery system (ENDS) products for sale without premarket authorization, in violation of the Family Smoking Prevention and Tobacco Control Act. The FDA determined the company's products qualified as tobacco products subject to FDA jurisdiction under the FD&C Act because they contained nicotine, and therefore required premarket authorization orders before legal marketing in the United States. The FDA identified that these ENDS products were being offered for sale or distribution through the company's website without the required compliance documentation.