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FDA Inspection 597811 — BioLife Plasma Services L.P.

BioLife Plasma Services L.P. — FEI 3007349296

The FDA completed an inspection of BioLife Plasma Services L.P. on June 24, 2009 in Sioux City, 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
June 24, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Sioux City, IA (United States)

Facility

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  • 990230 (NAI Tue Oct 18 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 920248 (NAI Tue Mar 24 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources