FDA Inspection 1283872 — Kazutomo Toyofuku

Kazutomo Toyofuku — FEI 3038548762

The FDA completed an inspection of Kazutomo Toyofuku on September 19, 2025 in Shinjuku. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 19, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Shinjuku (Japan)

Additional Details

Clinical Investigator (CI)