FDA Inspection 999368 — ImpactLife

ImpactLife — FEI 3003744945

The FDA completed an inspection of ImpactLife on January 19, 2017 in Macomb, IL. 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
January 19, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Macomb, IL (United States)