FDA inspection
LaserSight Technologies, Inc.: FDA inspection ending Jan 21, 2009
FDA inspection 562131 · Voluntary Action Indicated (VAI) · Winter Park, FL
Key facts
| Inspection ID | 562131 |
|---|---|
| Firm | LaserSight Technologies, Inc. |
| FEI number | 3002741596 |
| Address | 931 S. Semoran Boulevard |
| City | Winter Park |
| State | FL |
| ZIP | 32792 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jan 21, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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