FDA Inspection 792917 — Hantel Technologies Inc

Hantel Technologies Inc — FEI 3014382898

The FDA completed an inspection of Hantel Technologies Inc on July 24, 2012 in Hayward, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 24, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hayward, CA (United States)