FDA Inspection 549798 — Amerisourcebergen Drug Corporation

Amerisourcebergen Drug Corporation — FEI 3004388958

The FDA completed an inspection of Amerisourcebergen Drug Corporation on November 25, 2008 in Mansfield, MA. 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
November 25, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mansfield, MA (United States)