FDA Inspection 1043759 — Masru Kaneko

Masru Kaneko — FEI 3014063881

The FDA completed an inspection of Masru Kaneko on Feb 16, 2018 in Yokohama. 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 16, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Yokohama (Japan)

Additional Details

Clinical Investigator (CI)

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