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Vapemoreinc.com, Inc. was cited for offering electronic nicotine delivery system (ENDS) products for sale without required FDA premarket authorization. The company's website listed tobacco products containing nicotine that were not in compliance with the Family Smoking Prevention and Tobacco Control Act and FDA regulations under 21 C.F.R. § 1100.1. The FDA determined that as "new tobacco products," these ENDS products required premarket authorization orders before being legally marketed in the United States, which the company had failed to obtain.