FDA inspection
Arthrex California Technology: FDA inspection ending Oct 4, 2016
FDA inspection 996316 · Voluntary Action Indicated (VAI) · Santa Barbara, CA
Key facts
| Inspection ID | 996316 |
|---|---|
| Firm | Arthrex California Technology |
| FEI number | 3006990600 |
| Address | 460 Ward Dr |
| City | Santa Barbara |
| State | CA |
| ZIP | 93111-2356 |
| Fiscal year | 2017 |
| Inspection end date | Oct 4, 2016 |
| 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