FDA inspection
Laserworld USA Inc.: FDA inspection ending Mar 5, 2014
FDA inspection 871085 · No Action Indicated (NAI) · New York, NY
Key facts
| Inspection ID | 871085 |
|---|---|
| Firm | Laserworld USA Inc. |
| FEI number | 3010536806 |
| Address | 363 7th Ave Fl 6 |
| City | New York |
| State | NY |
| ZIP | 10001 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Mar 5, 2014 |
| Classification | No Action Indicated (NAI) |
| Project area | Radiation Control and Health Safety Act |
| 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