FDA Warning Letter — Kwik Trip 448

Case 694470 — FEI 3032524625

The FDA took a Warning Letter action against Kwik Trip 448 on Oct 8, 2024 (Minneapolis, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip 448
Date
Oct 8, 2024
Fiscal Year
2025
Product Type
Tobacco
Center
CTP
Location
Minneapolis, MN (United States)