# Osteomed, LLC, Addison, TX – FDA Inspections

Source: https://www.keypedia.com/companies/osteomed-llc/4b0582e3-14ed-4c50-b81e-eddb941a5531

> Inspection records and compliance data for Osteomed, LLC in Addison, Texas. 7 FDA inspections on record, 1 Form 483, last inspected August 08, 2025.

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## Details

- Name: Osteomed, LLC
- FEI Number: 2027754
- Address Line 1: 3885 Arapaho Rd
- City: Addison
- State: Texas
- Zip Code: 75001
- Country Name: United States
- Address: 3885 Arapaho Rd, Addison, Texas 75001, United States
- Country: United States

## Related Documents

- FDA Inspection 1278352 - Osteomed, LLC - 2025-08-08 — source: FDA, date: August 8, 2025
- FDA Inspection 1278352 - Osteomed, LLC - 2025-08-08 — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2025
- FDA Inspection 1278352 - Osteomed, LLC - 2025-08-08 — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2025
- FDA Inspection 1232268 - Osteomed, LLC - 2024-08-16 — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2024
- FDA Inspection 1217195 - Osteomed, LLC - 2023-08-28 — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2023
- FDA Inspection 1217195 - Osteomed, LLC - 2023-08-28 — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2023
- [FDA Inspection 1026378 - Osteomed, LLC - 2017-09-22](https://www.keypedia.com/records/fda_inspections/osteomed-llc/cce3738e-e82a-435b-9f7d-be72d6637cc2) — classification: No Action Indicated (NAI), source: FDA, date: September 22, 2017
- FDA Inspection 1026378 - Osteomed, LLC - 2017-09-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 22, 2017
- [FDA Inspection 955878 - Osteomed, LLC - 2016-01-07](https://www.keypedia.com/records/fda_inspections/osteomed-llc/47e43609-507a-42d7-84b1-44170e97322d) — classification: No Action Indicated (NAI), source: FDA, date: January 7, 2016
- FDA Inspection 868667 - Osteomed, LLC - 2014-02-28 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 28, 2014

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