FDA inspection
Glaukos Corporation: FDA inspection ending Mar 9, 2009
FDA inspection 562763 · Voluntary Action Indicated (VAI) · San Clemente, CA
Key facts
| Inspection ID | 562763 |
|---|---|
| Firm | Glaukos Corporation |
| FEI number | 3012341472 |
| Address | 229 Avenida Fabricante |
| City | San Clemente |
| State | CA |
| ZIP | 92672 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Mar 9, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring |
| 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