FDA inspection
DiaDexus, Inc: FDA inspection ending Sep 24, 2009
FDA inspection 619178 · Voluntary Action Indicated (VAI) · South San Francisco, CA
Key facts
| Inspection ID | 619178 |
|---|---|
| Firm | DiaDexus, Inc |
| FEI number | 3003643666 |
| Address | 349 Oyster Point Blvd |
| City | South San Francisco |
| State | CA |
| ZIP | 94080 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Sep 24, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 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