FDA Warning Letter — Ampride

Case 513794 — FEI 3013104526

The FDA took a Warning Letter action against Ampride on Dec 22, 2016 (Marengo, IA). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Ampride
Date
Dec 22, 2016
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Marengo, IA (United States)

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