# Anodyne Therapy, LLC – FDA Inspection, Sep 14, 2023

Source: https://www.keypedia.com/records/fda_inspections/anodyne-therapy-llc/9d68f084-038b-4789-943d-e74a90dcf4cf
Source feed: FDA_Inspections

> FDA inspection 1218240 of Anodyne Therapy, LLC, September 14, 2023. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1218240
- Company Name: Anodyne Therapy, LLC
- Inspection Date: 2023-09-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1314134 - 2026-04-22
- FDA Inspection 1116473 - 2020-01-23
- FDA Inspection 813482 - 2013-01-09
- FDA Inspection 578197 - 2009-04-17

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/ebony-d-sanon/703dc125-1019-43d1-9598-1bdc92026e2b)
- [Issuing Officer](https://www.keypedia.com/people/ulysses-d-singleton/e62f9da3-2c82-4ad7-910d-2da18144c789)

Company: https://www.keypedia.com/companies/anodyne-therapy-llc/ba888ab2-f3a6-47c7-9acb-e5bf59d750f1

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