FDA Inspection
Northgate Technologies, Inc.Northgate Technologies, Inc. – FDA Inspection, Nov 13, 2009
Record Details
This FDA Inspection record concerns Northgate Technologies, Inc., with an inspection on November 13, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Northgate Technologies, Inc.
- Inspection Date
- November 13, 2009
- Product Type
- Devices
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ID · f524e7b8-e6f2-4721-9a7e-f89ee8d3dbbe
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 636500
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.80(b)Incoming inspection, testing, verification
- 21 CFR 820.50(a)(1)Evaluation and Selection, Suppliers, Contractors, etc.
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Other FDA inspections of Northgate Technologies, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 19, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 1, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 3, 2012 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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