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Go Vapor LLC manufactured and distributed e-liquid 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 newly deemed tobacco products under the August 8, 2016 final rule, were required to have marketing authorization orders under section 910 of the Federal Food, Drug, and Cosmetic Act before being commercially distributed in the United States. The inspection revealed that Go Vapor LLC was operating in violation of FDA tobacco product regulations by failing to secure this mandatory premarket approval before offering their products for sale.