FDA Warning Letter — Accupack Midwest Inc

Case 680228 — FEI 1000122754

The FDA took a Warning Letter action against Accupack Midwest Inc on Aug 15, 2024 (Cincinnati, OH). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Accupack Midwest Inc
Date
Aug 15, 2024
Fiscal Year
2024
Product Type
Drugs
Center
CDER
Location
Cincinnati, OH (United States)

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