FDA Warning Letter — Kwik Trip 309

Case 677223 — FEI 3021374991

The FDA took a Warning Letter action against Kwik Trip 309 on Feb 6, 2024 (Burnsville, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip 309
Date
Feb 6, 2024
Fiscal Year
2024
Product Type
Tobacco
Center
CTP
Location
Burnsville, MN (United States)