FDA inspection
Arthrex, Inc.: FDA inspection ending Nov 30, 2018
FDA inspection 1101957 · Voluntary Action Indicated (VAI) · Naples, FL
Key facts
| Inspection ID | 1101957 |
|---|---|
| Firm | Arthrex, Inc. |
| FEI number | 1220246 |
| Address | 1370 Creekside Blvd |
| City | Naples |
| State | FL |
| ZIP | 34108-1945 |
| Fiscal year | 2019 |
| Inspection end date | Nov 30, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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
- 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