FDA Inspection
MicroVision, Inc.MicroVision, Inc. – FDA Inspection, Dec 20, 2012
Record Details
This FDA Inspection record concerns MicroVision, Inc., with an inspection on December 20, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- MicroVision, Inc.
- Inspection Date
- December 20, 2012
- Product Type
- Devices
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ID · d7f2f534-53e7-47ae-9c23-c86dbae1b932
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 812394
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(b)Documentation
- 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements
Full citation text and observation details available on the Dashboard.
Other FDA inspections of MicroVision, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 25, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| 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 |
| September 29, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for MicroVision, Inc.
- FDA Inspection 1206173 - 2023-05-25
- FDA Inspection 1105419 - 2019-10-03
- FDA Inspection 1036680 - 2017-12-06
- FDA Inspection 913515 - 2015-01-22
- FDA Inspection 615770 - 2009-09-29
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