FDA Inspection 793339 — Earest Inc

Earest Inc — FEI 3005936343

The FDA completed an inspection of Earest Inc on Jul 2, 2012 in Springfield, MO. 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
Jul 2, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Springfield, MO (United States)