FDA Inspection 948008 — ImpactLife

ImpactLife — FEI 3005754990

The FDA completed an inspection of ImpactLife on October 9, 2015 in Davenport, 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
October 9, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Davenport, IA (United States)