Lawrence Robert Ciardella
Apollo Future Technology, Inc.
4460 W Reno Ave Ste H-I
Las Vegas , NV 89118
United States
Support@apolloecigs.comFEI 3012691710Issued Aug 16, 2024Center for Tobacco Products
Source: FDA, published letter. FDA published this warning letter; View Letter opens FDA's copy. To check it, open FDA's record for this establishment, listed under FEI 3012691710.
Violations1
Issue DateAug 16, 2024
Product TypeTobacco
StatusOpen
Letter Details
Firm
Apollo Future Technology, Inc.
Location
Lawrence Robert Ciardella
Apollo Future Technology, Inc.
4460 W Reno Ave Ste H-I
Las Vegas , NV 89118
United States
Support@apolloecigs.com
FEI Number
3012691710
Country
United States
Issue Date
August 16, 2024
Issuing Office
Center for Tobacco Products
Product Type
Tobacco
Status
Open
Summary
Apollo Future Technology, Inc. was cited for offering electronic nicotine delivery system (ENDS) products for sale through its website without required premarket authorization from the FDA. The company's tobacco products, which contain nicotine from any source, failed to comply with the Federal Food, Drug, and Cosmetic Act and its implementing regulations governing new tobacco products. Under current FDA jurisdiction, which was expanded in March 2022 to include all nicotine-containing products regardless of source, the company was required to obtain premarket authorization orders before marketing these products in the United States.
Apollo Future Technology, Inc. FDA Warning Letter, August 16, 2024