FDA Warning Letter — Ampride

Case 509891 — FEI 3012810348

The FDA took a Warning Letter action against Ampride on Nov 3, 2016 (Cedar Falls, IA). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Ampride
Date
Nov 3, 2016
Fiscal Year
2017
Product Type
Tobacco
Center
CTP
Location
Cedar Falls, IA (United States)

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