# FDA Inspection 1020331 - MR Instruments Inc - August 02, 2017

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

> FDA Inspection 1020331 for MR Instruments Inc on August 02, 2017. Classification: No Action Indicated (NAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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