FDA Inspection 731362 — Kamiya Biomedical Company, LLC
The FDA completed an inspection of Kamiya Biomedical Company, LLC on Jun 15, 2011 in Tukwila, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 15, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Tukwila, WA (United States)