FDA Inspection 1062478 — Hirokazu Kitada, MD

Hirokazu Kitada, MD — FEI 3014454811

The FDA completed an inspection of Hirokazu Kitada, MD on Aug 2, 2018 in Osaka. 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
Aug 2, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Osaka (Japan)

Additional Details

Clinical Investigator (CI)