# Sense Technology Inc – FDA Inspection, Nov 6, 2017

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

> FDA inspection 1030739 of Sense Technology Inc, November 06, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 834226 - 2013-06-03
- FDA Inspection 717400 - 2011-03-28

## Related Officers

- [Company Rep](https://www.keypedia.com/people/brandon-l-mariner/c1ff0e66-552d-466a-9b49-a083d0211c94)
- [Company Rep](https://www.keypedia.com/people/dennis-r-hock/f13e2db1-b808-466d-a974-e5af2d5dfdb0)

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

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