FDA Inspection
Tenex Health, Inc.Tenex Health, Inc. – FDA Inspection, Nov 5, 2008
Record Details
This FDA Inspection record concerns Tenex Health, Inc., with an inspection on November 5, 2008, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Tenex Health, Inc.
- Inspection Date
- November 5, 2008
- Product Type
- Devices
View Company Profile
ID · eb4d29fa-37fb-4116-b281-86234cece7f7
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 543738
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Tenex Health, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| September 1, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 21, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 17, 2014 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 11, 2013 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 23, 2012 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Tenex Health, Inc.
- FDA Inspection 1152158 - 2021-09-01
- FDA Inspection 1023654 - 2017-08-21
- FDA Inspection 872655 - 2014-03-17
- FDA Inspection 822791 - 2013-04-11
- FDA Inspection 768795 - 2012-02-23
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