FDA Inspection 1281023 — Akihiro Kume, M.D.

Akihiro Kume, M.D. — FEI 3038549961

The FDA completed an inspection of Akihiro Kume, M.D. on September 4, 2025 in Sakai. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 4, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Sakai (Japan)

Additional Details

Clinical Investigator (CI)