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virginiavapes.com was warned for offering electronic nicotine delivery system (ENDS) products for sale without required premarket authorization under the Family Smoking Prevention and Tobacco Control Act. The FDA determined that the company's vaping products—classified as tobacco products under section 201(rr) of the FD&C Act because they contain nicotine—were being sold in violation of federal requirements that new tobacco products obtain premarket authorization orders before commercial marketing. The warning letter emphasized that since March 2022, FDA jurisdiction extends to all products containing nicotine from any source, requiring compliance regardless of whether the nicotine is derived from tobacco or synthetic sources.