FDA Inspection
Avery Dennison Belgie BVAvery Dennison Belgie BV – FDA Inspection, Apr 23, 2015
Record Details
This FDA Inspection record concerns Avery Dennison Belgie BV, with an inspection on April 23, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Avery Dennison Belgie BV
- Inspection Date
- April 23, 2015
- Product Type
- Devices
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ID · e5d65398-13f7-4a7b-8930-8286b1c97d0f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 931135
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 820.30(g)Design validation - user needs and intended uses
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Other FDA inspections of Avery Dennison Belgie BV
3| Date | Classification | Office | Project area |
|---|---|---|---|
| October 26, 2023 | Not classified | Office of Inspections and Investigations | |
| November 15, 2018 | Not classified | Office of Inspections and Investigations | |
| February 15, 2018 | Not classified | Office of Inspections and Investigations | Compliance: Devices |
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