FDA Warning Letter — QuikTrip

Case 535927 — FEI 3013731989

The FDA took a Warning Letter action against QuikTrip on August 24, 2017 (Olathe, KS). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
QuikTrip
Date
August 24, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Olathe, KS (United States)