FDA Inspection 1229492 — ImpactLife

ImpactLife — FEI 1470254

The FDA completed an inspection of ImpactLife on Aug 15, 2024 in Springfield, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 15, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Springfield, IL (United States)