FDA Inspection 1301186 — ImpactLife

ImpactLife — FEI 3005692903

The FDA completed an inspection of ImpactLife on February 2, 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
February 2, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cedar Rapids, IA (United States)