FDA Warning Letter — Kwik Trip
The FDA took a Warning Letter action against Kwik Trip on Aug 3, 2017 (Duluth, MN). The action was issued by CTP and concerns tobacco products.
Action Details
- Facility
- Kwik Trip
- Date
- Aug 3, 2017
- Fiscal Year
- 2017
- Product Type
- Tobacco
- Center
- CTP
- Location
- Duluth, MN (United States)