FDA Inspection 937275 — ImpactLife

ImpactLife — FEI 1970356

The FDA completed an inspection of ImpactLife on August 4, 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
August 4, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Davenport, IA (United States)