FDA Inspection 1228886 — Michio Yagi

Michio Yagi — FEI 3027960857

The FDA completed an inspection of Michio Yagi on Jan 25, 2024 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
Jan 25, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Osaka (Japan)

Additional Details

Clinical BA/BE

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