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FDA Inspection 849344 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 3006769911

The FDA completed an inspection of BioLife Plasma Services LP on September 20, 2013 in Moorhead, MN. 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 20, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Moorhead, MN (United States)

Facility

Other inspections at this facility

  • 1211185 (NAI Thu Jun 29 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1018617 (NAI Wed Jun 07 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 945442 (NAI Wed Sep 02 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 746370 (NAI Fri Sep 23 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 683983 (NAI Fri Sep 17 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources