FDA inspection

Dendreon Pharmaceuticals LLC: FDA inspection ending Nov 15, 2012

FDA inspection 848259 · Voluntary Action Indicated (VAI) · Seal Beach, CA

Key facts

Inspection ID 848259
Firm Dendreon Pharmaceuticals LLC
FEI number 3008821247
Address 1700 Saturn Way
City Seal Beach
State CA
ZIP 90740
Country United States
Fiscal year 2013
Inspection end date Nov 15, 2012
Classification Voluntary Action Indicated (VAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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