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FDA Inspection 1115611 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 1000143570

The FDA completed an inspection of BioLife Plasma Services LP on December 18, 2019 in Austin, TX. 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
December 18, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Austin, TX (United States)

Facility

Other inspections at this facility

  • 1027119 (NAI Wed Sep 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919736 (NAI Tue Mar 24 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 814072 (NAI Wed Jan 09 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 709258 (NAI Thu Feb 10 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 584544 (NAI Fri May 22 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources