FDA inspection
Lumasense Technologies, Inc.: FDA inspection ending May 2, 2003
FDA inspection 270768 · Voluntary Action Indicated (VAI) · Santa Clara, CA
Key facts
| Inspection ID | 270768 |
|---|---|
| Firm | Lumasense Technologies, Inc. |
| FEI number | 2936522 |
| Address | 3301 Leonard Ct |
| City | Santa Clara |
| State | CA |
| ZIP | 95054-2054 |
| Fiscal year | 2003 |
| Inspection end date | May 2, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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