FDA Inspection 1228231 — ImpactLife

ImpactLife — FEI 1937912

The FDA completed an inspection of ImpactLife on January 30, 2024 in Burlington, 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 30, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Burlington, IA (United States)