Loading…
Drive Thru Vapors, LLC manufactured and distributed e-liquid tobacco products without obtaining required premarket authorization from the FDA, violating the Family Smoking Prevention and Tobacco Control Act. The company's e-liquid products, classified as electronic nicotine delivery systems under FDA jurisdiction since August 2016, were adulterated and misbranded because they lacked the mandatory marketing authorization for new tobacco products required under section 910 of the Federal Food, Drug, and Cosmetic Act. The FDA determined the company was commercially distributing these tobacco products in the United States without the legally mandated premarket approval.