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FDA Warning Letter — QuikTrip

Case 717630 — FEI 3013731989

The FDA took a Warning Letter action against QuikTrip on Sep 30, 2025 (Olathe, KS). The action was issued by CTP and concerns tobacco products.

Action details

Facility
QuikTrip
Date
Sep 30, 2025
Fiscal Year
2025
Product Type
Tobacco
Center
CTP
Location
Olathe, KS (United States)

Facility

Other compliance actions

FDA data resources

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