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FDA Inspection 552395 — BioLife Plasma Services, L.P.

BioLife Plasma Services, L.P. — FEI 3000717651

The FDA completed an inspection of BioLife Plasma Services, L.P. on December 22, 2008 in Janesville, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 22, 2008
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Janesville, WI (United States)

Facility

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  • 845930 (NAI Thu Aug 22 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources