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FDA Inspection 1025481 — BioLife Plasma Services, L.P

BioLife Plasma Services, L.P — FEI 1876544

The FDA completed an inspection of BioLife Plasma Services, L.P on September 6, 2017 in Bloomington, IN. 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
September 6, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bloomington, IN (United States)

Facility

Other inspections at this facility

  • 1200795 (NAI Thu Mar 16 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 836455 (NAI Thu Jun 06 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 728133 (NAI Thu Jun 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources