FDA Inspection 1222354 — Kaneka Corporation

Kaneka Corporation — FEI 3002807368

The FDA completed an inspection of Kaneka Corporation on Oct 13, 2023 in Takasago-Cho. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 13, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Takasago-Cho (Japan)