FDA Warning Letter — Mini Quick Mart

Case 571923 — FEI 3015082901

The FDA took a Warning Letter action against Mini Quick Mart on Jan 10, 2019 (Milwaukee, WI). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Mini Quick Mart
Date
Jan 10, 2019
Fiscal Year
2019
Product Type
Tobacco
Center
CTP
Location
Milwaukee, WI (United States)

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