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FDA Inspection 746861 — Accupack Midwest Inc

Accupack Midwest Inc — FEI 1000122754

The FDA completed an inspection of Accupack Midwest Inc on September 16, 2011 in Cincinnati, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 16, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cincinnati, OH (United States)

Facility

Other inspections at this facility

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  • 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))
  • 610579 (VAI Wed Aug 12 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources