# FDA Inspection 1030739 - Sense Technology Inc - November 06, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/sense-technology-inc/80c882ef-bc8a-428b-b420-b27d36c9877b
Source feed: FDA_Inspections

> FDA Inspection 1030739 for Sense Technology Inc on November 06, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030739
- Company Name: Sense Technology Inc
- Inspection Date: 2017-11-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 834226 - 2013-06-03](https://www.globalkeysolutions.net/records/fda_inspections/sense-technology-inc/1b2e98f7-8dc8-4f18-8e6f-054bc8381ed7)
- [FDA Inspection 834226 - 2013-06-03](https://www.globalkeysolutions.net/records/fda_inspections/sense-technology-inc/40a46bf1-dbc3-462d-b908-c26afdbc9580)
- [FDA Inspection 717400 - 2011-03-28](https://www.globalkeysolutions.net/records/fda_inspections/sense-technology-inc/10170b20-181a-4acd-9df0-9ac4378fd44d)
- [FDA Inspection 717400 - 2011-03-28](https://www.globalkeysolutions.net/records/fda_inspections/sense-technology-inc/c689d1e1-830a-4a07-861d-7083cd9a7ad1)

Company: https://www.globalkeysolutions.net/companies/sense-technology-inc/b6c78ded-2772-41eb-9dd0-5f797a931b12

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7