Big News: FDA is moving from MasterControl to ComplianceQuest.See Why
Talk to a SpecialistLoading…
Talk to a SpecialistTalk to a SpecialistRuthless Vapor Corporation was cited for manufacturing and distributing electronic nicotine delivery system (ENDS) products without the required premarket authorization orders mandated by the Federal Food, Drug, and Cosmetic Act. The FDA determined that products listed on the company's websites (ruthlessvapor.com and ruthlesswholesale.com) were tobacco products subject to FDA jurisdiction, including those containing nicotine from non-tobacco sources following the March 2022 legislative expansion of FDA authority. The company failed to comply with FD&C Act requirements applicable to new tobacco products that were not commercially marketed in the United States as of February 15, 2007.