# Sintx Technologies Inc – FDA Inspection, Mar 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/sintx-technologies-inc/bf61caed-d5f5-4a06-9673-377abf3afa6e
Source feed: FDA_Inspections

> FDA inspection 1007302 of Sintx Technologies Inc, March 10, 2017. Classification: Voluntary Action Indicated (VAI). 6 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: 1007302
- Company Name: Sintx Technologies Inc
- Inspection Date: 2017-03-10
- 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: 6

## Related Documents

- [FDA Inspection 879329 - 2014-05-09](https://www.keypedia.com/records/fda_inspections/sintx-technologies-inc/81f3d7f0-7517-4beb-aea5-77c8d318449d)
- [FDA Inspection 724895 - 2011-05-13](https://www.keypedia.com/records/fda_inspections/sintx-technologies-inc/7b52015d-3e47-4f70-8421-f9ccf18deea7)

## Related Officers

- [Investigator](https://www.keypedia.com/people/kathleen-s-tormey/5e1abfe2-078a-4c61-bb98-3885f853a945)
- [FDA Associated Person](https://www.keypedia.com/people/vicky-l-cruz/282da571-56be-48f4-96c6-d590829b12c2)

Company: https://www.keypedia.com/companies/sintx-technologies-inc/76601667-b9b4-48d1-8615-b2019b0693ac

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