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FDA Inspection 620196 — AmerisourceBergen Drug Corporation

AmerisourceBergen Drug Corporation — FEI 2112794

The FDA completed an inspection of AmerisourceBergen Drug Corporation on September 30, 2009 in Shakopee, MN. 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 30, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Shakopee, MN (United States)

Facility

Other inspections at this facility

  • 1287260 (NAI Tue Sep 09 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 800947 (NAI Fri Sep 14 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 604080 (NAI Mon Aug 03 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources