FDA Inspection 1028514 — BioLife Plasma Services, L.P.

BioLife Plasma Services, L.P. — FEI 3010569471

The FDA completed an inspection of BioLife Plasma Services, L.P. on September 20, 2017 in Fort Wayne, IN. 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
September 20, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fort Wayne, IN (United States)