FDA Inspection 1100877 — Octapharma Plasma Inc
The FDA completed an inspection of Octapharma Plasma Inc on August 14, 2019 in Northlake, IL. 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
- August 14, 2019
- Fiscal Year
- 2019
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Northlake, IL (United States)