FDA Warning Letter — Kwik Trip

Case 512296 — FEI 3013006857

The FDA took a Warning Letter action against Kwik Trip on Dec 8, 2016 (Dakota, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Dec 8, 2016
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Dakota, MN (United States)