FDA Inspection 1234158 — Kan Yonemori, M.D.

Kan Yonemori, M.D. — FEI 3030078726

The FDA completed an inspection of Kan Yonemori, M.D. on Mar 7, 2024 in Chuo. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 7, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chuo (Japan)

Additional Details

Clinical Investigator (CI)

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