FDA inspection
Synthes (USA) Products LLC: FDA inspection ending Apr 27, 2009
FDA inspection 583439 · Voluntary Action Indicated (VAI) · West Chester, PA
Key facts
| Inspection ID | 583439 |
|---|---|
| Firm | Synthes (USA) Products LLC |
| FEI number | 3008812560 |
| Address | 1303 Goshen Pkwy |
| City | West Chester |
| State | PA |
| ZIP | 19380 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Apr 27, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
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
- 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