FDA inspection
Glaukos Corporation: FDA inspection ending Jun 10, 2016
FDA inspection 981961 · Voluntary Action Indicated (VAI) · San Clemente, CA
Key facts
| Inspection ID | 981961 |
|---|---|
| Firm | Glaukos Corporation |
| FEI number | 3012341472 |
| Address | 26051 Merit Cir Ste 103 |
| City | San Clemente |
| State | CA |
| ZIP | 92672 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Jun 10, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None 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