FDA Warning Letter — Kwik Trip

Case 523570 — FEI 3013457124

The FDA took a Warning Letter action against Kwik Trip on Apr 27, 2017 (Rochester, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Apr 27, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Rochester, MN (United States)