FDA inspection
OriGen Biomedical, Inc.: FDA inspection ending Apr 26, 2013
FDA inspection 828408 · Voluntary Action Indicated (VAI) · Austin, TX
Key facts
| Inspection ID | 828408 |
|---|---|
| Firm | OriGen Biomedical, Inc. |
| FEI number | 1000160256 |
| Address | 7000 Burleson Rd Bldg D |
| City | Austin |
| State | TX |
| ZIP | 78744 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Apr 26, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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