FDA Inspection 621836 — Umed Corporation

Umed Corporation — FEI 3005792406

The FDA completed an inspection of Umed Corporation on Jan 21, 2009 in Bartlett, 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 21, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Bartlett, IL (United States)