FDA Inspection 671674 — Kaneka Corporation

Kaneka Corporation — FEI 3002807368

The FDA completed an inspection of Kaneka Corporation on Jun 3, 2010 in Takasago-Cho. 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
Jun 3, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Takasago-Cho (Japan)