# FDA Inspection 1314134 - Anodyne Therapy, LLC - April 22, 2026

Source: https://www.globalkeysolutions.net/records/fda_inspections/anodyne-therapy-llc/dd006cd4-a783-451b-a793-6e192c28446d
Source feed: FDA_Inspections

> FDA Inspection 1314134 for Anodyne Therapy, LLC on April 22, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1314134
- Company Name: Anodyne Therapy, LLC
- Inspection Date: 2026-04-22
- 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 1314134 - 2026-04-22](https://www.globalkeysolutions.net/records/fda_inspections/anodyne-therapy-llc/f732c7e4-4794-4415-8e08-cb487e4b43b7)
- [FDA Inspection 1218240 - 2023-09-14](https://www.globalkeysolutions.net/records/fda_inspections/anodyne-therapy-llc/9d68f084-038b-4789-943d-e74a90dcf4cf)
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Company: https://www.globalkeysolutions.net/companies/anodyne-therapy-llc/ba888ab2-f3a6-47c7-9acb-e5bf59d750f1

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