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FDA Warning Letter — Circle K

Case 568520 — FEI 3014853528

The FDA took a Warning Letter action against Circle K on Nov 8, 2018 (Denver, CO). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Circle K
Date
Nov 8, 2018
Fiscal Year
2019
Product Type
Tobacco
Center
CTP
Location
Denver, CO (United States)

Facility

Other compliance actions

FDA data resources

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