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FDA Inspection 1116650 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 1978019

The FDA completed an inspection of BioLife Plasma Services LP on January 31, 2020 in Springfield, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 31, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Springfield, MO (United States)

Facility

Other inspections at this facility

  • 1009867 (NAI Thu Apr 20 2017 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