FDA Inspection 1277670 — Accupack Midwest Inc

Accupack Midwest Inc — FEI 1000122754

The FDA completed an inspection of Accupack Midwest Inc on Jul 23, 2025 in Cincinnati, OH. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Jul 23, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cincinnati, OH (United States)

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