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FDA Inspection 833620 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 3007959978

The FDA completed an inspection of BioLife Plasma Services LP on May 30, 2013 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
May 30, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cedar Falls, IA (United States)

Facility

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FDA data resources