FDA Inspection 1258920 — BioLife Plasma Services

BioLife Plasma Services — FEI 3013906372

The FDA completed an inspection of BioLife Plasma Services on Jan 16, 2025 in Mount Juliet, TN. 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
Jan 16, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mount Juliet, TN (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.