FDA Inspection 870344 — Baxalta US Inc.

Baxalta US Inc. — FEI 1000519965

The FDA completed an inspection of Baxalta US Inc. on February 28, 2014 in Thousand Oaks, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 28, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Thousand Oaks, CA (United States)