# Sintx Technologies Inc – FDA Inspection, May 13, 2011

Source: https://www.keypedia.com/records/fda_inspections/sintx-technologies-inc/7b52015d-3e47-4f70-8421-f9ccf18deea7
Source feed: FDA_Inspections

> FDA inspection 724895 of Sintx Technologies Inc, May 13, 2011. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803, 806 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 724895
- Company Name: Sintx Technologies Inc
- Inspection Date: 2011-05-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- [FDA Inspection 1007302 - 2017-03-10](https://www.keypedia.com/records/fda_inspections/sintx-technologies-inc/bf61caed-d5f5-4a06-9673-377abf3afa6e)
- [FDA Inspection 879329 - 2014-05-09](https://www.keypedia.com/records/fda_inspections/sintx-technologies-inc/81f3d7f0-7517-4beb-aea5-77c8d318449d)

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