FDA Inspection
MR Instruments IncMR Instruments Inc – FDA Inspection, Aug 2, 2017
Record Details
This FDA Inspection record concerns MR Instruments Inc, with an inspection on August 2, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 6fe8b7ad-26aa-40e4-b1a8-f8e024e8733f
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1020331
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of MR Instruments Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 26, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 12, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for MR Instruments Inc
- FDA Inspection 1180261 - 2022-08-26
- FDA Inspection 748117 - 2011-09-12
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