# FDA Inspection 1007302 - Sintx Technologies Inc - March 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 for Sintx Technologies Inc on March 10, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 879329 - 2014-05-09](https://www.keypedia.com/records/fda_inspections/sintx-technologies-inc/4c78ab59-fe87-4a9f-b35c-95785f5c0c58)
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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