# FDA 483 - BURTON MEDICAL - February 20, 2026

Source: https://www.keypedia.com/records/483/burton-medical/d946f15f-fed9-44f8-b16e-a14eac4ba639

> FDA 483 for BURTON MEDICAL on February 20, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: BURTON MEDICAL
- Inspection Date: 2026-02-20
- Product Type: device
- Office Name: FDA District Office — Chicago, Illinois
- Summary: An FDA inspection of BURTON MEDICAL in Addison, IL, a manufacturer of medical devices, identified one significant observation. The firm failed to provide required information to the Global Unique Device Identification Database by not registering its APEX LED Class II surgical light device. This indicates a compliance issue related to device identification and tracking.

## Related Documents

- [483 - 2019-10-30](https://www.keypedia.com/records/483/burton-medical/413205f2-bd32-4769-8834-672b4c07f71a)

## Related Officers

- [Hammam A. Abdallah](https://www.keypedia.com/people/hammam-a-abdallah/fc1ee5c3-b00c-43af-b5a3-1bdc2ad6c5d7)

Company: https://www.keypedia.com/companies/burton-medical/4cd7a15c-6124-4d31-8f3f-f3f3c5f38c08

Office: https://www.keypedia.com/offices/fda-district-office-chicago-illinois/62c2811c-10c5-4d74-99d0-eb5047ef3b65