FDA Inspection 551596 — Numotech Inc

Numotech Inc — FEI 1000518730

The FDA completed an inspection of Numotech Inc on Nov 21, 2008 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
Nov 21, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Northridge, CA (United States)

Citations

IDCFRDescription
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
341521 CFR 820.22Quality Audit/Reaudit - conducted