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FDA Inspection 1030469 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 1937444

The FDA completed an inspection of BioLife Plasma Services LP on October 16, 2017 in Coralville, IA. 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
October 16, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Coralville, IA (United States)

Facility

Other inspections at this facility

  • 1202521 (NAI Wed Apr 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 952159 (NAI Wed Dec 16 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 874160 (NAI Fri Apr 11 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 769007 (NAI Thu Jan 26 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 648129 (NAI Wed Feb 24 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources