FDA Inspection 1115050 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3013771915

The FDA completed an inspection of CSL Plasma Inc. on Nov 14, 2019 in Mckeesport, PA. 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
Nov 14, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mckeesport, PA (United States)

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