# MR Instruments Inc – FDA Inspection, Aug 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/mr-instruments-inc/6fe8b7ad-26aa-40e4-b1a8-f8e024e8733f
Source feed: FDA_Inspections

> FDA inspection 1020331 of MR Instruments Inc, August 02, 2017. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020331
- Company Name: MR Instruments Inc
- Inspection Date: 2017-08-02
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1180261 - 2022-08-26](https://www.keypedia.com/records/fda_inspections/mr-instruments-inc/eaeae084-c7aa-4f68-9772-3cd7a78cea1a)
- FDA Inspection 748117 - 2011-09-12

## Related Officers

- [Company Rep](https://www.keypedia.com/people/jennifer-s-ness/532f8a81-e393-4e83-b5f2-a72362e966de)

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