FDA inspection
Xitron Technologies Inc: FDA inspection ending May 5, 2006
FDA inspection 426026 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 426026 |
|---|---|
| Firm | Xitron Technologies Inc |
| FEI number | 1000125441 |
| Address | 5959 Cornerstone Ct W Ste 100 |
| City | San Diego |
| State | CA |
| ZIP | 92121-3764 |
| Fiscal year | 2006 |
| Inspection end date | May 5, 2006 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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