FDA Inspection
Allied Vision Group IncAllied Vision Group Inc – FDA Inspection, Apr 22, 2022
Record Details
This FDA Inspection record concerns Allied Vision Group Inc, with an inspection on April 22, 2022, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Allied Vision Group Inc
- Inspection Date
- April 22, 2022
- Product Type
- Devices
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ID · b864589a-671f-4375-b2b8-7cc761176cda
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1167949
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
6- 21 CFR 820.160(b)Distribution records
- 21 CFR 820.25(b)Training records
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.50(a)(1)Documented evaluation
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Other FDA inspections of Allied Vision Group Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 21, 2019 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 11, 2018 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
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