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FDA Warning Letter — QuikTrip

Case 512248 — FEI 3013012083

The FDA took a Warning Letter action against QuikTrip on Dec 8, 2016 (Omaha, NE). The action was issued by CTP and concerns tobacco products.

Action details

Facility
QuikTrip
Date
Dec 8, 2016
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Omaha, NE (United States)

Facility

Other compliance actions

FDA data resources

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