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Vaproma Inc. was warned for offering electronic nicotine delivery system (ENDS) products for sale on its website without the required premarket authorization orders mandated by the Federal Food, Drug, and Cosmetic Act. The FDA determined that these products qualify as tobacco products subject to FDA jurisdiction because they contain nicotine from any source, including the synthetic nicotine covered under legislation enacted in March 2022 that expanded the definition of regulated tobacco products. The company failed to comply with section 910(a) of the FD&C Act, which requires all new tobacco products to obtain premarket approval before being legally marketed in the United States.