FDA Warning Letter — Kwik Trip 465

Case 699858 — FEI 3034045492

The FDA took a Warning Letter action against Kwik Trip 465 on Jan 7, 2025 (Minneapolis, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip 465
Date
Jan 7, 2025
Fiscal Year
2025
Product Type
Tobacco
Center
CTP
Location
Minneapolis, MN (United States)