FDA Inspection 1159489 — BioLife Plasma Services, LP

BioLife Plasma Services, LP — FEI 3017161003

The FDA completed an inspection of BioLife Plasma Services, LP on Dec 14, 2021 in Baltimore, MD. 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
Dec 14, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Baltimore, MD (United States)