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FDA Inspection 1277670 — Accupack Midwest Inc

Accupack Midwest Inc — FEI 1000122754

The FDA completed an inspection of Accupack Midwest Inc on July 23, 2025 in Cincinnati, OH. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

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

Facility

Other inspections at this facility

  • 1231139 (OAI Tue Feb 27 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 980166 (VAI Fri Jun 17 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 803394 (VAI Thu Oct 11 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 746861 (VAI Fri Sep 16 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 610579 (VAI Wed Aug 12 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources