FDA Warning Letter — Quik Mart/Citgo

Case 519356 — FEI 3013321282

The FDA took a Warning Letter action against Quik Mart/Citgo on Mar 9, 2017 (Detroit, MI). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Quik Mart/Citgo
Date
Mar 9, 2017
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Detroit, MI (United States)

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