FDA Inspection 848259 — Dendreon Pharmaceuticals LLC

Dendreon Pharmaceuticals LLC — FEI 3008821247

The FDA completed an inspection of Dendreon Pharmaceuticals LLC on November 15, 2012 in Seal Beach, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 15, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Seal Beach, CA (United States)