FDA Warning Letter — Quick Mart

Case 640106 — FEI 3023626474

The FDA took a Warning Letter action against Quick Mart on Aug 18, 2022 (Dundalk, MD). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Quick Mart
Date
Aug 18, 2022
Fiscal Year
2022
Product Type
Tobacco
Center
CTP
Location
Dundalk, MD (United States)