FDA Inspection 1028823 — CSL Plasma Inc.
The FDA completed an inspection of CSL Plasma Inc. on Oct 5, 2017 in Landover, MD. 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
- Oct 5, 2017
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Landover, MD (United States)