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FDA Inspection 1086933 — BioLife Plasma Services, L.P.

BioLife Plasma Services, L.P. — FEI 3001614614

The FDA completed an inspection of BioLife Plasma Services, L.P. on April 4, 2019 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
April 4, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mankato, MN (United States)

Facility

Other inspections at this facility

  • 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))
  • 701875 (NAI Wed Dec 01 2010 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