FDA Inspection 921394 — ImpactLife

ImpactLife — FEI 1470270

The FDA completed an inspection of ImpactLife on March 26, 2015 in Urbana, IL. 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
March 26, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Urbana, IL (United States)