FDA Inspection 1108055 — ImpactLife

ImpactLife — FEI 3003319042

The FDA completed an inspection of ImpactLife on September 14, 2019 in Galesburg, 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
September 14, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Galesburg, IL (United States)