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FDA Inspection 1034333 — Biolife Plasma Services LP

Biolife Plasma Services LP — FEI 3008133911

The FDA completed an inspection of Biolife Plasma Services LP on December 6, 2017 in Middletown, OH. 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 6, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Middletown, OH (United States)

Facility

Other inspections at this facility

  • 1119614 (NAI Thu Feb 27 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 946553 (NAI Fri Oct 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 855043 (NAI Thu Nov 14 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 741509 (NAI Thu Aug 25 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources