FDA inspection
AlloSource Inc.: FDA inspection ending Aug 14, 2012
FDA inspection 796666 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 796666 |
|---|---|
| Firm | AlloSource Inc. |
| FEI number | 3002851781 |
| Address | 7436 Mission Valley Rd |
| City | San Diego |
| State | CA |
| ZIP | 92108 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Aug 14, 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
- 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