FDA Inspection 835125 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1978022

The FDA completed an inspection of CSL Plasma Inc. on Jun 7, 2013 in Springfield, MO. 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
Jun 7, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Springfield, MO (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.