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FDA Inspection 1009867 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 1978019

The FDA completed an inspection of BioLife Plasma Services LP on April 20, 2017 in Springfield, MO. 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
April 20, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Springfield, MO (United States)

Facility

Other inspections at this facility

  • 1116650 (VAI Fri Jan 31 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 939857 (NAI Wed Aug 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 835124 (NAI Wed Jun 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 721776 (NAI Thu May 12 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources