FDA Inspection 955640 — BioLife Plasma Services L.P.

BioLife Plasma Services L.P. — FEI 1000218225

The FDA completed an inspection of BioLife Plasma Services L.P. on Jan 15, 2016 in Cedar Rapids, IA. 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 15, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cedar Rapids, IA (United States)