FDA inspection
Dynavax Technologies Corporation: FDA inspection ending Oct 17, 2012
FDA inspection 804781 · Voluntary Action Indicated (VAI) · Emeryville, CA
Key facts
| Inspection ID | 804781 |
|---|---|
| Firm | Dynavax Technologies Corporation |
| FEI number | 3003212117 |
| Address | 2100 Powell St Ste 900 |
| City | Emeryville |
| State | CA |
| ZIP | 94608 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Oct 17, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring |
| 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