FDA Inspection 1200649 — ImpactLife

ImpactLife — FEI 3003960009

The FDA completed an inspection of ImpactLife on March 22, 2023 in Dubuque, 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
March 22, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Dubuque, IA (United States)