FDA Inspection 1031496 — Dendreon Pharmaceuticals LLC

Dendreon Pharmaceuticals LLC — FEI 3008914686

The FDA completed an inspection of Dendreon Pharmaceuticals LLC on November 1, 2016 in Union City, GA. 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 1, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Union City, GA (United States)