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FDA Inspection 1028806 — BioLife Plasma Services L.P.

BioLife Plasma Services L.P. — FEI 1876578

The FDA completed an inspection of BioLife Plasma Services L.P. on September 28, 2017 in Muncie, IN. 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 28, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Muncie, IN (United States)

Facility

Other inspections at this facility

  • 1117248 (NAI Fri Jan 24 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 837107 (NAI Wed Jun 19 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 732175 (NAI Wed Jun 29 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources