FDA inspection
STRYKER IRELAND OSTEONICS: FDA inspection ending May 21, 2009
FDA inspection 590920 · Voluntary Action Indicated (VAI) · Carrigtwohill, County Cork
Key facts
| Inspection ID | 590920 |
|---|---|
| Firm | STRYKER IRELAND OSTEONICS |
| FEI number | 3002459190 |
| Address | Tullagreen Building, IDA Business & Technology Park, Carrigtwohill Industrial Estate |
| City | Carrigtwohill, County Cork |
| Country | Ireland |
| Fiscal year | 2009 |
| Inspection end date | May 21, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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