# FDA Inspection 1302476 - AR Fabricating - February 11, 2026

Source: https://www.keypedia.com/records/fda_inspections/ar-fabricating/034bce39-2472-4742-9a07-dbdb1fc6958e
Source feed: FDA_Inspections

> FDA Inspection 1302476 for AR Fabricating on February 11, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1302476
- Company Name: AR Fabricating
- Inspection Date: 2026-02-11
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Dallas District Office

## Related Documents

- [FDA Inspection 1302476 - 2026-02-11](https://www.keypedia.com/records/fda_inspections/ar-fabricating/3cdb68f5-e9df-4c94-8a58-4d1f86d35eb1)
- [FDA Inspection 1302476 - 2026-02-11](https://www.keypedia.com/records/fda_inspections/ar-fabricating/59b9ec41-8900-49a3-bffc-36ce79d76afa)
- [FDA Inspection 1302476 - 2026-02-11](https://www.keypedia.com/records/fda_inspections/ar-fabricating/f379a07b-12f0-4532-96a6-2f61759a7a0c)

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