FDA Inspection 1055650 — Hisashi Hidaka, M.D.

Hisashi Hidaka, M.D. — FEI 3014199157

The FDA completed an inspection of Hisashi Hidaka, M.D. on May 10, 2018 in Kanagawa. 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
May 10, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Kanagawa (Japan)

Additional Details

Clinical Investigator (CI)