FDA Inspection 916099 — Kamiya Biomedical Company, LLC

Kamiya Biomedical Company, LLC — FEI 2084025

The FDA completed an inspection of Kamiya Biomedical Company, LLC on Feb 26, 2015 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
Feb 26, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Tukwila, WA (United States)