FDA inspection
Stryker Medical Division of Stryker Corporation: FDA inspection ending May 15, 2009
FDA inspection 584103 · Official Action Indicated (OAI) · Portage, MI
Key facts
| Inspection ID | 584103 |
|---|---|
| Firm | Stryker Medical Division of Stryker Corporation |
| FEI number | 1831750 |
| Address | 3800 E Centre Ave |
| City | Portage |
| State | MI |
| ZIP | 49002 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | May 15, 2009 |
| Classification | Official Action Indicated (OAI) |
| 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
- 10–99 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