FDA inspection
Dendreon Pharmaceuticals LLC: FDA inspection ending Jan 22, 2016
FDA inspection 961300 · Voluntary Action Indicated (VAI) · Seal Beach, CA
Key facts
| Inspection ID | 961300 |
|---|---|
| Firm | Dendreon Pharmaceuticals LLC |
| FEI number | 3008821247 |
| Address | 1700 Saturn Way |
| City | Seal Beach |
| State | CA |
| ZIP | 90740 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Jan 22, 2016 |
| 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