FDA inspection
Alcon Refractive Horizons, Inc.: FDA inspection ending Jan 12, 2000
FDA inspection 10038 · No Action Indicated (NAI) · Orlando, FL
Key facts
| Inspection ID | 10038 |
|---|---|
| Firm | Alcon Refractive Horizons, Inc. |
| FEI number | 3000209733 |
| Address | 2501 and 2800 Discovery Drive |
| City | Orlando |
| State | FL |
| ZIP | 32826-3010 |
| Fiscal year | 2000 |
| Inspection end date | Jan 12, 2000 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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