FDA Inspection 903067 — ImpactLife

ImpactLife — FEI 3009588529

The FDA completed an inspection of ImpactLife on October 21, 2014 in Cedar Rapids, 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 21, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cedar Rapids, IA (United States)