FDA inspection
Lightmed USA Inc: FDA inspection ending Jan 28, 2009
FDA inspection 580472 · No Action Indicated (NAI) · San Clemente, CA
Key facts
| Inspection ID | 580472 |
|---|---|
| Firm | Lightmed USA Inc |
| FEI number | 3003976404 |
| Address | 1130 Calle Cordillera Ste 101 |
| City | San Clemente |
| State | CA |
| ZIP | 92673 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jan 28, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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