FDA Warning Letter — KWIK TRIP 806

Case 575193 — FEI 3015176422

The FDA took a Warning Letter action against KWIK TRIP 806 on Feb 28, 2019 (Owatonna, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
KWIK TRIP 806
Date
Feb 28, 2019
Fiscal Year
2019
Product Type
Tobacco
Center
CTP
Location
Owatonna, MN (United States)