FDA Warning Letter — Circle K

Case 512347 — FEI 3013038423

The FDA took a Warning Letter action against Circle K on Dec 8, 2016 (Saginaw, MI). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Circle K
Date
Dec 8, 2016
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Saginaw, MI (United States)

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