FDA Warning Letter — Kwik Trip

Case 520576 — FEI 3013322255

The FDA took a Warning Letter action against Kwik Trip on Mar 23, 2017 (Lake City, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Mar 23, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Lake City, MN (United States)