FDA Inspection 694961 — ImpactLife

ImpactLife — FEI 3000719226

The FDA completed an inspection of ImpactLife on Oct 25, 2010 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
Oct 25, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mattoon, IL (United States)