FDA Inspection
Anodyne Therapy, LLCAnodyne Therapy, LLC – FDA Inspection, Sep 14, 2023
Record Details
This FDA Inspection record concerns Anodyne Therapy, LLC, with an inspection on September 14, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 9d68f084-038b-4789-943d-e74a90dcf4cf
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1218240
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Anodyne Therapy, LLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| April 22, 2026 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 23, 2020 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| January 9, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 17, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Anodyne Therapy, LLC
- FDA Inspection 1314134 - 2026-04-22
- FDA Inspection 1116473 - 2020-01-23
- FDA Inspection 813482 - 2013-01-09
- FDA Inspection 578197 - 2009-04-17
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