FDA Inspection 658365 — Lifesource Mundelein
The FDA completed an inspection of Lifesource Mundelein on Apr 8, 2010 in Mundelein, IL. 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
- Apr 8, 2010
- Fiscal Year
- 2010
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Mundelein, IL (United States)