FDA Inspection 628951 — LifeSource Joliet

LifeSource Joliet — FEI 3005172099

The FDA completed an inspection of LifeSource Joliet on Nov 18, 2009 in Joliet, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 18, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Joliet, IL (United States)