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FDA Inspection 701875 — BioLife Plasma Services, L.P.

BioLife Plasma Services, L.P. — FEI 3001614614

The FDA completed an inspection of BioLife Plasma Services, L.P. on December 1, 2010 in Mankato, 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
December 1, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mankato, MN (United States)

Facility

Other inspections at this facility

  • 1086933 (NAI Thu Apr 04 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 931626 (NAI Thu Jun 11 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 811689 (NAI Wed Dec 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 563356 (NAI Wed Jan 21 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources