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FDA Inspection 1040704 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 3007959978

The FDA completed an inspection of BioLife Plasma Services LP on August 30, 2017 in Cedar Falls, IA. 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
August 30, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cedar Falls, IA (United States)

Facility

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  • 1151821 (NAI Wed Aug 11 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 913597 (NAI Thu Feb 12 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 833620 (NAI Thu May 30 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 713684 (NAI Fri Mar 11 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources