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Atomic Vapor, an e-liquid manufacturer in Canon City, Colorado, was warned that its tobacco products required premarket authorization under the Family Smoking Prevention and Tobacco Control Act but lacked the necessary marketing authorization orders. The company's e-liquid products, classified as electronic nicotine delivery systems under FDA jurisdiction since the August 2016 deeming rule, were being manufactured and distributed commercially without compliance with Federal Food, Drug, and Cosmetic Act requirements. The FDA determined the products were adulterated and/or misbranded due to the absence of required premarket approval for these "new tobacco products" that were not commercially marketed in the United States prior to February 15, 2007.