FDA Warning Letter — Kwik Trip

Case 534618 — FEI 3011545140

The FDA took a Warning Letter action against Kwik Trip on Aug 10, 2017 (Eyota, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Kwik Trip
Date
Aug 10, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Eyota, MN (United States)