FDA Inspection 1234288 — Keiji Ozeki, M.D.

Keiji Ozeki, M.D. — FEI 3029889506

The FDA completed an inspection of Keiji Ozeki, M.D. on Feb 29, 2024 in Nagoya. 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
Feb 29, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Nagoya (Japan)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.