FDA Inspection 1298962 — ImpactLife

ImpactLife — FEI 3009588529

The FDA completed an inspection of ImpactLife on January 15, 2026 in Cedar Rapids, IA. 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 15, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cedar Rapids, IA (United States)