FDA Warning Letter — QuikTrip

Case 512149 — FEI 3013008503

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)

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