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FDA Inspection 804871 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 1938048

The FDA completed an inspection of BioLife Plasma Services LP on October 25, 2012 in Dubuque, 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 25, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Dubuque, IA (United States)

Facility

Other inspections at this facility

  • 1150292 (NAI Wed Aug 25 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 992755 (NAI Wed Nov 09 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 927306 (NAI Mon May 11 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 902666 (NAI Wed Oct 29 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 697937 (NAI Wed Nov 10 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources