FDA Inspection 828387 — ImpactLife

ImpactLife — FEI 3000719226

The FDA completed an inspection of ImpactLife on Apr 22, 2013 in Mattoon, IL. 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, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mattoon, IL (United States)