FDA Inspection 904783 — Galena Biopharma, Inc.

Galena Biopharma, Inc. — FEI 3011078156

The FDA completed an inspection of Galena Biopharma, Inc. on November 21, 2014 in San Ramon, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 21, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
San Ramon, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)