FDA Warning Letter — Kwik Trip

Case 526474 — FEI 3013557924

The FDA took a Warning Letter action against Kwik Trip on Jun 8, 2017 (Mankato, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Jun 8, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Mankato, MN (United States)