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FDA Inspection 1122260 — BioLIfe Plasma Services L.P.

BioLIfe Plasma Services L.P. — FEI 3004014548

The FDA completed an inspection of BioLIfe Plasma Services L.P. on January 15, 2020 in Dekalb, IL. 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
January 15, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Dekalb, IL (United States)

Facility

Other inspections at this facility

  • 1031323 (NAI Thu Oct 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 938634 (NAI Fri Aug 14 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 915796 (NAI Mon Sep 22 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources