FDA Inspection 633570 — Astellas Pharma Inc.

Astellas Pharma Inc. — FEI 3002808523

The FDA completed an inspection of Astellas Pharma Inc. on October 15, 2009 in Takahagi. 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
October 15, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Takahagi (Japan)