FDA Inspection
Ivoclar Vivadent AGIvoclar Vivadent AG – FDA Inspection, Aug 24, 2016
Record Details
This FDA Inspection record concerns Ivoclar Vivadent AG, with an inspection on August 24, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Ivoclar Vivadent AG
- Inspection Date
- August 24, 2016
- Product Type
- Devices
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ID · 82a35996-096c-44d6-9368-f7db474ac5bc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 988253
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of Ivoclar Vivadent AG
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 27, 2018 | Not classified | Office of Inspections and Investigations |
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