FDA Inspection 1258774 — CSL Plasma Inc.
The FDA completed an inspection of CSL Plasma Inc. on Jan 10, 2025 in Hobart, IN. 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
- Jan 10, 2025
- Fiscal Year
- 2025
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Hobart, IN (United States)