# FDA 483 - AR Fabricating - February 11, 2026

Source: https://www.keypedia.com/records/483/ar-fabricating/a92fce5d-53ce-400d-a0ea-f149ca821684

> FDA 483 for AR Fabricating on February 11, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: AR Fabricating
- Inspection Date: 2026-02-11
- Product Type: device
- Office Name: Dallas District Office
- Summary: An FDA inspection of AR Fabricating in Georgetown, TX, a manufacturer of Class II medical devices, revealed significant deficiencies in their quality system. The firm failed to adequately validate critical manufacturing processes, lacked documented procedures for key production controls, and did not properly evaluate or monitor its suppliers. These issues indicate a systemic breakdown in ensuring product quality and safety.

## Related Officers

- [Katlin N. Stubbs](https://www.keypedia.com/people/katlin-n-stubbs/27d70db1-a2e9-4254-a721-c6de655f7626)

Company: https://www.keypedia.com/companies/ar-fabricating/df5f813e-dc41-4dc3-be2d-34b29764b790

Office: https://www.keypedia.com/offices/dallas-district-office/2d1ee9ae-c44c-4494-8186-a920a69b98f9