# FDA Inspection 543738 - Tenex Health, Inc. - November 05, 2008

Source: https://www.keypedia.com/records/fda_inspections/tenex-health-inc/2968982d-8ac9-4c4f-81c7-783149e112a3
Source feed: FDA_Inspections

> FDA Inspection 543738 for Tenex Health, Inc. on November 05, 2008. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 543738
- Company Name: Tenex Health, Inc.
- Inspection Date: 2008-11-05
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1152158 - 2021-09-01](https://www.keypedia.com/records/fda_inspections/tenex-health-inc/3833fdb1-7791-41d0-96a5-0232a423a6c2)
- [FDA Inspection 1152158 - 2021-09-01](https://www.keypedia.com/records/fda_inspections/tenex-health-inc/b192ddcd-3a11-4f69-9b2a-9243cdf05198)
- [FDA Inspection 1023654 - 2017-08-21](https://www.keypedia.com/records/fda_inspections/tenex-health-inc/6997bb05-62a1-4c9b-8b4a-a65f11743144)
- [FDA Inspection 872655 - 2014-03-17](https://www.keypedia.com/records/fda_inspections/tenex-health-inc/afcca3cb-e6f4-47f5-bfe9-945722ca34b1)
- [FDA Inspection 872655 - 2014-03-17](https://www.keypedia.com/records/fda_inspections/tenex-health-inc/6ba39516-ed00-440a-8fda-adfe1e8b4f2c)

Company: https://www.keypedia.com/companies/tenex-health-inc/465ce143-879b-4361-84f5-d44bb953f66c

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