FDA Inspection
Neurovision Medical Products IncNeurovision Medical Products Inc – FDA Inspection, Nov 20, 2012
Record Details
This FDA Inspection record concerns Neurovision Medical Products Inc, with an inspection on November 20, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- November 20, 2012
- Product Type
- Devices
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ID · 67ebc317-af83-4c35-abc5-ed3a61793d55
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 810024
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
- 21 CFR 820.90(b)(2)Product rework documentation, DHR {see also 820.184}
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Other FDA inspections of Neurovision Medical Products Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 13, 2024 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 30, 2016 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 22, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Neurovision Medical Products Inc
- FDA Inspection 1234182 - 2024-02-13
- FDA Inspection 986763 - 2016-09-30
- FDA Inspection 681607 - 2010-09-22
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