# FDA Inspection 1180261 - MR Instruments Inc - August 26, 2022

Source: https://www.keypedia.com/records/fda_inspections/mr-instruments-inc/eaeae084-c7aa-4f68-9772-3cd7a78cea1a
Source feed: FDA_Inspections

> FDA Inspection 1180261 for MR Instruments Inc on August 26, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180261
- Company Name: MR Instruments Inc
- Inspection Date: 2022-08-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1180261 - 2022-08-26](https://www.keypedia.com/records/fda_inspections/mr-instruments-inc/909c7044-e4b4-419c-ba74-47f5bc5a1f4f)
- [FDA Inspection 1020331 - 2017-08-02](https://www.keypedia.com/records/fda_inspections/mr-instruments-inc/6fe8b7ad-26aa-40e4-b1a8-f8e024e8733f)
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Company: https://www.keypedia.com/companies/mr-instruments-inc/77d23b60-ab30-429b-a11f-0a2395fb286f

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