FDA inspection
Xlumena, Inc.: FDA inspection ending Jan 16, 2013
FDA inspection 813140 · Voluntary Action Indicated (VAI) · Mountain View, CA
Key facts
| Inspection ID | 813140 |
|---|---|
| Firm | Xlumena, Inc. |
| FEI number | 3008516478 |
| Address | 453 Ravendale Dr Ste H |
| City | Mountain View |
| State | CA |
| ZIP | 94043 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Jan 16, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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