FDA Inspection 1297342 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 3028001508

The FDA completed an inspection of BioLife Plasma Services LP on December 18, 2025 in Chicago, 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
December 18, 2025
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Chicago, IL (United States)