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Great American Vapes Bossier City was warned for manufacturing and distributing e-liquid tobacco products without obtaining required premarket authorization under the Family Smoking Prevention and Tobacco Control Act. The company failed to comply with FDA regulations governing newly deemed tobacco products, specifically electronic nicotine delivery systems that became subject to FDA jurisdiction effective August 8, 2016. The products were determined to be unapproved "new tobacco products" that required premarket authorization before commercial distribution in the United States.