FDA Inspection 682676 — Numotech Inc

Numotech Inc — FEI 1000518730

The FDA completed an inspection of Numotech Inc on Sep 20, 2010 in Northridge, CA. 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
Sep 20, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Northridge, CA (United States)