FDA Inspection 875787 — ImpactLife

ImpactLife — FEI 1970361

The FDA completed an inspection of ImpactLife on Apr 22, 2014 in Ottumwa, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 22, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Ottumwa, IA (United States)