FDA Inspection 977294 — ImpactLife

ImpactLife — FEI 1970356

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