# FDA Inspection 1192937 - Minnetronix, Inc. - December 08, 2022

Source: https://www.keypedia.com/records/fda_inspections/minnetronix-inc/a842e26e-5e08-43ff-8b83-8d9cf55bcc7d
Source feed: FDA_Inspections

> FDA Inspection 1192937 for Minnetronix, Inc. on December 08, 2022. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1192937
- Company Name: Minnetronix, Inc.
- Inspection Date: 2022-12-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1310502 - 2026-04-01](https://www.keypedia.com/records/fda_inspections/minnetronix-inc/d2137322-ce03-4bbd-a4d2-d92a763e760f)
- [FDA Inspection 1272311 - 2025-06-04](https://www.keypedia.com/records/fda_inspections/minnetronix-inc/81d895da-2693-4ca4-92b5-3fda1978905c)
- [FDA Inspection 1215791 - 2023-08-08](https://www.keypedia.com/records/fda_inspections/minnetronix-inc/049b69c7-e762-4f0e-b2cb-023e550cf625)
- [FDA Inspection 1089675 - 2019-04-10](https://www.keypedia.com/records/fda_inspections/minnetronix-inc/cc5ca6e4-6874-4826-9d92-a7c4fc7f39c4)
- [FDA Inspection 1016466 - 2017-05-11](https://www.keypedia.com/records/fda_inspections/minnetronix-inc/48e87a26-2272-4789-8def-a0fe8a879d56)

Company: https://www.keypedia.com/companies/minnetronix-inc/81340393-b77e-4542-ac34-af2289dc65d6

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7