# Anodyne Therapy, LLC, Oldsmar, FL – FDA Inspections

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

> Inspection records and compliance data for Anodyne Therapy, LLC in Oldsmar, Florida. 5 FDA inspections on record, last inspected April 22, 2026.

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## Details

- Name: Anodyne Therapy, LLC
- FEI Number: 1000113231
- Address Line 1: 301b Mears Blvd
- City: Oldsmar
- State: Florida
- Zip Code: 34677
- Country Name: United States
- Address: 301b Mears Blvd, Oldsmar, Florida 34677, United States
- Country: United States

## Related Documents

- FDA Inspection 1314134 - Anodyne Therapy, LLC - 2026-04-22 — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2026
- FDA Inspection 1314134 - Anodyne Therapy, LLC - 2026-04-22 — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2026
- FDA Inspection 1218240 - Anodyne Therapy, LLC - 2023-09-14 — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2023
- [FDA Inspection 1218240 - Anodyne Therapy, LLC - 2023-09-14](https://www.keypedia.com/records/fda_inspections/anodyne-therapy-llc/9d68f084-038b-4789-943d-e74a90dcf4cf) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2023
- FDA Inspection 1116473 - Anodyne Therapy, LLC - 2020-01-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 23, 2020
- FDA Inspection 1116473 - Anodyne Therapy, LLC - 2020-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2020
- FDA Inspection 1116473 - Anodyne Therapy, LLC - 2020-01-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 23, 2020
- FDA Inspection 813482 - Anodyne Therapy, LLC - 2013-01-09 — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2013
- FDA Inspection 813482 - Anodyne Therapy, LLC - 2013-01-09 — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2013
- FDA Inspection 578197 - Anodyne Therapy, LLC - 2009-04-17 — classification: No Action Indicated (NAI), source: FDA, date: April 17, 2009

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