FDA Inspection 1110448 — Amane Kozuki MD

Amane Kozuki MD — FEI 3015592949

The FDA completed an inspection of Amane Kozuki MD on October 25, 2019 in Osaka. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 25, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Osaka (Japan)

Additional Details

Clinical Investigator (CI)