FDA Inspection 611304 — BioLife Plasma Services, L.P.

BioLife Plasma Services, L.P. — FEI 3003419404

The FDA completed an inspection of BioLife Plasma Services, L.P. on July 31, 2009 in Missoula, MT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 31, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Missoula, MT (United States)

Citations

IDCFRDescription
16121 CFR 606.160(a)(2)Determination of lot numbers and supplies
7621 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs