FDA Inspection 645965 — Axiom Marketing Inc

Axiom Marketing Inc — FEI 3005985361

The FDA completed an inspection of Axiom Marketing Inc on Jan 20, 2010 in Lake Forest, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 20, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Lake Forest, IL (United States)