FDA Inspection 1315930 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 3015521860

The FDA completed an inspection of BioLife Plasma Services LP on May 4, 2026 in Phoenix, AZ. 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
May 4, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Phoenix, AZ (United States)