FDA Inspection 1004210 — Numotech Inc

Numotech Inc — FEI 1000518730

The FDA completed an inspection of Numotech Inc on Mar 6, 2017 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
Mar 6, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Northridge, CA (United States)