FDA inspection
NuVasive Inc: FDA inspection ending May 26, 2017
FDA inspection 1011810 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 1011810 |
|---|---|
| Firm | NuVasive Inc |
| FEI number | 3002980729 |
| Address | 7475 Lusk Blvd |
| City | San Diego |
| State | CA |
| ZIP | 92121 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | May 26, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
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