FDA Inspection 756552 — Astellas Pharma Inc.

Astellas Pharma Inc. — FEI 3002807001

The FDA completed an inspection of Astellas Pharma Inc. on November 21, 2011 in Takaoka. 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
November 21, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Takaoka (Japan)