FDA Inspection 1037918 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3011273912

The FDA completed an inspection of CSL Plasma Inc. on December 6, 2017 in Murfreesboro, TN. 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
December 6, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Murfreesboro, TN (United States)