FDA Inspection 697937 — BioLife Plasma Services LP

BioLife Plasma Services LP — FEI 1938048

The FDA completed an inspection of BioLife Plasma Services LP on November 10, 2010 in Dubuque, 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
November 10, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Dubuque, IA (United States)