FDA Inspection 824920 — Numotech Inc

Numotech Inc — FEI 1000518730

The FDA completed an inspection of Numotech Inc on Apr 1, 2013 in Northridge, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 1, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Northridge, CA (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures