FDA Inspection 1068869 — LifeSource Crystal Lake

LifeSource Crystal Lake — FEI 3005627420

The FDA completed an inspection of LifeSource Crystal Lake on Aug 7, 2018 in Crystal Lake, 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
Aug 7, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Crystal Lake, IL (United States)