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FDA Warning Letter — QuikTrip 239

Case 667646 — FEI 3028208801

The FDA took a Warning Letter action against QuikTrip 239 on Sep 19, 2023 (Kansas City, KS). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
QuikTrip 239
Date
Sep 19, 2023
Fiscal Year
2023
Product Type
Tobacco
Center
CTP
Location
Kansas City, KS (United States)

Facility

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.