FDA inspection
Synthes (USA) Products LLC: FDA inspection ending Oct 17, 2017
FDA inspection 1032557 · No Action Indicated (NAI) · West Chester, PA
Key facts
| Inspection ID | 1032557 |
|---|---|
| Firm | Synthes (USA) Products LLC |
| FEI number | 3008812560 |
| Address | 1301 Goshen Pkwy |
| City | West Chester |
| State | PA |
| ZIP | 19380 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Oct 17, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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