FDA inspection
Nevro Corporation: FDA inspection ending May 2, 2013
FDA inspection 832134 · Voluntary Action Indicated (VAI) · Redwood City, CA
Key facts
| Inspection ID | 832134 |
|---|---|
| Firm | Nevro Corporation |
| FEI number | 3008514029 |
| Address | 1800 Bridge Pkwy |
| City | Redwood City |
| State | CA |
| ZIP | 94065 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | May 2, 2013 |
| 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
- 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