FDA Inspection
MicroVision, Inc.MicroVision, Inc. – FDA Inspection, May 25, 2023
Record Details
This FDA Inspection record concerns MicroVision, Inc., with an inspection on May 25, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · a56ebc65-cf3c-4c97-bff2-4b43dc7b3205
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1206173
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
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Other FDA inspections of MicroVision, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| October 3, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 6, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 22, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 20, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 29, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for MicroVision, Inc.
- FDA Inspection 1105419 - 2019-10-03
- FDA Inspection 1036680 - 2017-12-06
- FDA Inspection 913515 - 2015-01-22
- FDA Inspection 812394 - 2012-12-20
- FDA Inspection 615770 - 2009-09-29
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