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FDA Inspection 770123 — Biolife Plasma Services

Biolife Plasma Services — FEI 1876554

The FDA completed an inspection of Biolife Plasma Services on February 28, 2012 in Grand Rapids, MI. 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
February 28, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grand Rapids, MI (United States)

Facility

Other inspections at this facility

  • 1142760 (NAI Thu May 20 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1013345 (NAI Thu Apr 27 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 868868 (NAI Fri Mar 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 653623 (NAI Tue Mar 23 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources