FDA Inspection 638132 — Hantel Technologies Inc

Hantel Technologies Inc — FEI 3014382898

The FDA completed an inspection of Hantel Technologies Inc on January 6, 2010 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
January 6, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Hayward, CA (United States)