# Omnia Medical - Inspection Records

Source: https://www.keypedia.com/companies/omnia-medical/231109bd-5403-4992-861c-72049445d381

> Inspection records and compliance data for Omnia Medical in Morgantown, West Virginia. Access full analysis and detailed observations.

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## Details

- Name: Omnia Medical
- FEI Number: 3010560653
- City: Morgantown
- State: West Virginia
- Country Name: United States
- Address Line 1: 6 Canyon Rd Ste 300
- Zip Code: 26508

## Related Documents

- [483 - Omnia Medical - 2025-07-28](https://www.keypedia.com/records/483/omnia-medical/96e6ca20-f92d-4a77-b3b9-967982060653) — source: FDA, date: July 28, 2025
- [483 - Omnia Medical - 2025-07-28](https://www.keypedia.com/records/483/omnia-medical/999532c0-ced9-4806-8131-7ae5ed9196c1) — source: FDA, date: July 28, 2025
- [FDA Inspection 1276815 - Omnia Medical - 2025-07-28](https://www.keypedia.com/records/fda_inspections/omnia-medical/8497c891-a1a4-44da-b9fb-72eb6036b6af) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 28, 2025
- [FDA Inspection 1276815 - Omnia Medical - 2025-07-28](https://www.keypedia.com/records/fda_inspections/omnia-medical/1919632b-d4c8-46f5-80e0-6333bdbc74f1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 28, 2025
- [FDA Inspection 1276815 - Omnia Medical - 2025-07-28](https://www.keypedia.com/records/fda_inspections/omnia-medical/89eacf67-1b90-465c-a8cc-32746e8dd143) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 28, 2025
- [FDA Inspection 1276815 - Omnia Medical - 2025-07-28](https://www.keypedia.com/records/fda_inspections/omnia-medical/d8816e3d-85e0-4749-a377-78886b96e8ef) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 28, 2025
- [FDA Inspection 1082466 - Omnia Medical - 2019-02-06](https://www.keypedia.com/records/fda_inspections/omnia-medical/000cf922-5b19-47e4-8970-b8ec611ed505) — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2019
- [FDA Inspection 1082466 - Omnia Medical - 2019-02-06](https://www.keypedia.com/records/fda_inspections/omnia-medical/5fa1f90d-93fa-4b17-b4b6-6f39237fec95) — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2019

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## Related Officers

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