FDA inspection
Stryker Instruments Div. of Stryker Corporation: FDA inspection ending Sep 1, 2005
FDA inspection 399543 · No Action Indicated (NAI) · Portage, MI
Key facts
| Inspection ID | 399543 |
|---|---|
| Firm | Stryker Instruments Div. of Stryker Corporation |
| FEI number | 1811755 |
| Address | 4100 E Milham Ave |
| City | Portage |
| State | MI |
| ZIP | 49002-9704 |
| Fiscal year | 2005 |
| Inspection end date | Sep 1, 2005 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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