# FDA Inspection 1283810 - Mirodx - September 26, 2025

Source: https://www.keypedia.com/records/fda_inspections/mirodx/fcce9bd0-e46a-4f04-9676-1ec37ef51721
Source feed: FDA_Inspections

> FDA Inspection 1283810 for Mirodx on September 26, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1283810
- Company Name: Mirodx
- Inspection Date: 2025-09-26
- 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 1283810 - 2025-09-26](https://www.keypedia.com/records/fda_inspections/mirodx/7002813b-5335-4ba3-bcd7-c934ed6ff119)
- [FDA Inspection 1283810 - 2025-09-26](https://www.keypedia.com/records/fda_inspections/mirodx/9b529446-dbed-4440-8a0a-da37ca9814b2)
- [FDA Inspection 1283810 - 2025-09-26](https://www.keypedia.com/records/fda_inspections/mirodx/a8f3ae68-3371-4e65-9c6a-6f3a803a6b9b)

Company: https://www.keypedia.com/companies/mirodx/32dd43f8-f43f-4cc4-9d4e-6df9bf2dfce1

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