FDA Inspection 958347 — CSL Plasma Inc.
The FDA completed an inspection of CSL Plasma Inc. on February 1, 2016 in Roseville, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 1, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Roseville, MI (United States)