FDA Warning Letter — Kwik Trip

Case 523136 — FEI 3013438498

The FDA took a Warning Letter action against Kwik Trip on Apr 20, 2017 (Byron, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Apr 20, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Byron, MN (United States)