FDA inspection
Corixa Corporation: FDA inspection ending May 13, 2015
FDA inspection 938930 · Voluntary Action Indicated (VAI) · Marietta, PA
Key facts
| Inspection ID | 938930 |
|---|---|
| Firm | Corixa Corporation |
| FEI number | 3007726770 |
| Address | 325 N Bridge St |
| City | Marietta |
| State | PA |
| ZIP | 17547 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | May 13, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Vaccines and Allergenic Products |
| Product type | Biologics |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 10–99 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