FDA Warning Letter — Kwik Trip 392
The FDA took a Warning Letter action against Kwik Trip 392 on Oct 3, 2024 (Ripon, WI). The action was issued by CTP and concerns tobacco products.
Action Details
- Facility
- Kwik Trip 392
- Date
- Oct 3, 2024
- Fiscal Year
- 2025
- Product Type
- Tobacco
- Center
- CTP
- Location
- Ripon, WI (United States)