FDA Inspection 1062734 — Csl Plasma, Inc.

Csl Plasma, Inc. — FEI 2177738

The FDA completed an inspection of Csl Plasma, Inc. on Jul 18, 2018 in Minneapolis, MN. 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
Jul 18, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Minneapolis, MN (United States)