FDA inspection
Vertebral Technologies, Inc.: FDA inspection ending Jun 12, 2009
FDA inspection 588231 · No Action Indicated (NAI) · Santa Clara, CA
Key facts
| Inspection ID | 588231 |
|---|---|
| Firm | Vertebral Technologies, Inc. |
| FEI number | 3007617183 |
| Address | 2344 Walsh Ave |
| City | Santa Clara |
| State | CA |
| ZIP | 95051 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jun 12, 2009 |
| Classification | No Action Indicated (NAI) |
| 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