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My Vpro was found to be offering electronic nicotine delivery system (ENDS) products for sale on its website without the required premarket authorization from the FDA, in violation of the Family Smoking Prevention and Tobacco Control Act. The company failed to comply with FDA regulations requiring that "new tobacco products" obtain a marketing authorization order before being legally marketed in the United States, regardless of whether the nicotine source was derived from tobacco or another source. The Center for Tobacco Products determined that the ENDS products listed on myvpro.com were unapproved tobacco products subject to FDA jurisdiction under section 901(b) of the Federal Food, Drug, and Cosmetic Act and its implementing regulations.