# Sontec Instruments, Inc – FDA Inspection, Oct 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/sontec-instruments-inc/14a0f6d0-8957-4626-b794-9110938aac16
Source feed: FDA_Inspections

> FDA inspection 991205 of Sontec Instruments, Inc, October 21, 2016. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991205
- Company Name: Sontec Instruments, Inc
- Inspection Date: 2016-10-21
- 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: 7

## Related Officers

- [Investigator](https://www.keypedia.com/people/kathleen-s-tormey/5e1abfe2-078a-4c61-bb98-3885f853a945)
- [Company Rep](https://www.keypedia.com/people/matthew-m-vernon/f77e8c18-8614-49e3-9b19-3327b7fe7648)

Company: https://www.keypedia.com/companies/sontec-instruments-inc/24776cc8-6cb9-409d-bf36-95f2bf3e290e

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