FDA inspection
Endologix, Inc.: FDA inspection ending May 24, 2019
FDA inspection 1091013 · Voluntary Action Indicated (VAI) · Santa Rosa, CA
Key facts
| Inspection ID | 1091013 |
|---|---|
| Firm | Endologix, Inc. |
| FEI number | 3008011247 |
| Address | 3910 Brickway Blvd |
| City | Santa Rosa |
| State | CA |
| ZIP | 95403 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | May 24, 2019 |
| 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