FDA Inspection 1027835 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3011015567

The FDA completed an inspection of CSL Plasma Inc. on September 20, 2017 in Hillsboro, OR. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 20, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Hillsboro, OR (United States)