FDA Warning Letter — Kwik Trip 397
The FDA took a Warning Letter action against Kwik Trip 397 on May 3, 2018 (Saint Paul, MN). The action was issued by CTP and concerns tobacco products.
Action Details
- Facility
- Kwik Trip 397
- Date
- May 3, 2018
- Fiscal Year
- 2018
- Product Type
- Tobacco
- Center
- CTP
- Location
- Saint Paul, MN (United States)