FDA Inspection 1241704 — Kamiya Biomedical Company, LLC

Kamiya Biomedical Company, LLC — FEI 2084025

The FDA completed an inspection of Kamiya Biomedical Company, LLC on May 16, 2024 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
May 16, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tukwila, WA (United States)