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FDA Warning Letter — QuikTrip

Case 537936 — FEI 3013828018

The FDA took a Warning Letter action against QuikTrip on Sep 21, 2017 (Des Moines, IA). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
QuikTrip
Date
Sep 21, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Des Moines, IA (United States)

Facility

FDA data resources

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