FDA Inspection 638132 — Hantel Technologies Inc
The FDA completed an inspection of Hantel Technologies Inc on Jan 6, 2010 in Hayward, 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
- Jan 6, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Hayward, CA (United States)