FDA Inspection 1292866 — Shiono Finesse, Ltd.

Shiono Finesse, Ltd. — FEI 3005940219

The FDA completed an inspection of Shiono Finesse, Ltd. on October 24, 2025 in Sakai. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 24, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sakai (Japan)