FDA Inspection 661446 — Baxalta US Inc.

Baxalta US Inc. — FEI 3000121413

The FDA completed an inspection of Baxalta US Inc. on May 13, 2010 in Westlake Village, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 13, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Westlake Village, CA (United States)

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