# Tenex Health, Inc. – FDA Inspection, Mar 17, 2014

Source: https://www.keypedia.com/records/fda_inspections/tenex-health-inc/afcca3cb-e6f4-47f5-bfe9-945722ca34b1
Source feed: FDA_Inspections

> FDA inspection 872655 of Tenex Health, Inc., March 17, 2014. Classification: Official Action Indicated (OAI). 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 872655
- Company Name: Tenex Health, Inc.
- Inspection Date: 2014-03-17
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1152158 - 2021-09-01
- FDA Inspection 1023654 - 2017-08-21
- [FDA Inspection 822791 - 2013-04-11](https://www.keypedia.com/records/fda_inspections/tenex-health-inc/f8daac20-d4a7-431a-bc0d-8428b77db71e)
- [FDA Inspection 768795 - 2012-02-23](https://www.keypedia.com/records/fda_inspections/tenex-health-inc/79767a44-8848-49e3-90d5-309212b198fd)
- FDA Inspection 625866 - 2009-11-02

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