FDA inspection
Nevro Corporation: FDA inspection ending Aug 13, 2025
FDA inspection 1276522 · Official Action Indicated (OAI) · Redwood City, CA
Key facts
| Inspection ID | 1276522 |
|---|---|
| Firm | Nevro Corporation |
| FEI number | 3008514029 |
| Address | 1800 Bridge Pkwy |
| City | Redwood City |
| State | CA |
| ZIP | 94065 |
| Country | United States |
| Fiscal year | 2025 |
| Inspection end date | Aug 13, 2025 |
| Classification | Official Action Indicated (OAI) |
| Project area | Postmarket Assurance: Devices |
| 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