FDA Inspection
Ivoclar Vivadent Manufacturing GmbHIvoclar Vivadent Manufacturing GmbH – FDA Inspection, Sep 6, 2018
Record Details
This FDA Inspection record concerns Ivoclar Vivadent Manufacturing GmbH, with an inspection on September 6, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- September 6, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 51c11016-1c85-4e87-bd09-b99e5dca9d74
Inspection Facts
- Inspection number
- 1124028
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Ivoclar Vivadent Manufacturing GmbH
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 26, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 5, 2010 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Ivoclar Vivadent Manufacturing GmbH
- FDA Inspection 988687 - 2016-08-26
- FDA Inspection 681145 - 2010-08-05
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