FDA Inspection 1008323 — ImpactLife

ImpactLife — FEI 3005752939

The FDA completed an inspection of ImpactLife on January 26, 2017 in Maryville, 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
January 26, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Maryville, IL (United States)