FDA Inspection 562581 — AmeriSourceBergen Drug Corporation

AmeriSourceBergen Drug Corporation — FEI 3004459493

The FDA completed an inspection of AmeriSourceBergen Drug Corporation on January 6, 2009 in Conshohocken, PA. 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
January 6, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Postmarket Surv. and Epidemiology
Location
Conshohocken, PA (United States)