FDA Inspection 904330 — ImpactLife

ImpactLife — FEI 3004157291

The FDA completed an inspection of ImpactLife on Nov 21, 2014 in Earth City, MO. 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
Nov 21, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Earth City, MO (United States)