FDA Inspection 659259 — ImpactLife

ImpactLife — FEI 3003319042

The FDA completed an inspection of ImpactLife on Apr 27, 2010 in Galesburg, 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
Apr 27, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Galesburg, IL (United States)

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