FDA inspection
Arthrex Manufacturing Inc: FDA inspection ending Mar 24, 2017
FDA inspection 1026560 · Voluntary Action Indicated (VAI) · Ave Maria, FL
Key facts
| Inspection ID | 1026560 |
|---|---|
| Firm | Arthrex Manufacturing Inc |
| FEI number | 3010331645 |
| Address | 6875 Arthrex Commerce Dr |
| City | Ave Maria |
| State | FL |
| ZIP | 34142-9534 |
| Fiscal year | 2017 |
| Inspection end date | Mar 24, 2017 |
| 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
- 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