FDA Inspection 1331840 — BioLife Plasma Service L.P.

BioLife Plasma Service L.P. — FEI 3022484878

The FDA completed an inspection of BioLife Plasma Service L.P. on Aug 12, 2026 in Rockford, 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
Aug 12, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Rockford, IL (United States)