FDA inspection
Kamiya Biomedical Company, LLC: FDA inspection ending Dec 16, 2008
FDA inspection 554423 · No Action Indicated (NAI) · Tukwila, WA
Key facts
| Inspection ID | 554423 |
|---|---|
| Firm | Kamiya Biomedical Company, LLC |
| FEI number | 2084025 |
| Address | 12779 Gateway Dr S |
| City | Tukwila |
| State | WA |
| ZIP | 98168 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Dec 16, 2008 |
| 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