FDA Inspection 1323474 — Nippon Kayaku Co., Ltd.

Nippon Kayaku Co., Ltd. — FEI 3002807722

The FDA completed an inspection of Nippon Kayaku Co., Ltd. on May 29, 2026 in Takasaki. 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
May 29, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Takasaki (Japan)