FDA Warning Letter — Quik Trip

Case 526871 — FEI 3013564701

The FDA took a Warning Letter action against Quik Trip on Jun 15, 2017 (Urbandale, IA). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Quik Trip
Date
Jun 15, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Urbandale, IA (United States)

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