FDA Warning Letter — Quiktrip 541
The FDA took a Warning Letter action against Quiktrip 541 on Aug 9, 2018 (Des Moines, IA). The action was issued by CTP and concerns tobacco products.
Action Details
- Facility
- Quiktrip 541
- Date
- Aug 9, 2018
- Fiscal Year
- 2018
- Product Type
- Tobacco
- Center
- CTP
- Location
- Des Moines, IA (United States)