FDA Inspection 1068603 — BioLife Plasma Services L.P.

BioLife Plasma Services L.P. — FEI 3011638482

The FDA completed an inspection of BioLife Plasma Services L.P. on Sep 28, 2018 in Ankeny, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 28, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Ankeny, IA (United States)