FDA Inspection 543589 — AmerisourceBergen Drug Corporation

AmerisourceBergen Drug Corporation — FEI 3001238831

The FDA completed an inspection of AmerisourceBergen Drug Corporation on October 16, 2008 in Kansas City, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 16, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kansas City, MO (United States)