FDA Inspection 724861 — Omron Healthcare Inc

Omron Healthcare Inc — FEI 3008919616

The FDA completed an inspection of Omron Healthcare Inc on May 17, 2011 in Alsip, 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
May 17, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Alsip, IL (United States)