FDA Inspection 940490 — Galena Biopharma, Inc.

Galena Biopharma, Inc. — FEI 3011078156

The FDA completed an inspection of Galena Biopharma, Inc. on August 25, 2015 in San Ramon, CA. 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
August 25, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Postmarket Surv. and Epidemiology
Location
San Ramon, CA (United States)