FDA Inspection 770005 — Astellas Pharma Inc.

Astellas Pharma Inc. — FEI 3002807003

The FDA completed an inspection of Astellas Pharma Inc. on February 10, 2012 in Toyama. 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
February 10, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Toyama (Japan)