FDA Inspection
Ivoclar Vivadent Manufacturing, Inc.Ivoclar Vivadent Manufacturing, Inc. – FDA Inspection, Jan 21, 2009
Record Details
This FDA Inspection record concerns Ivoclar Vivadent Manufacturing, Inc., with an inspection on January 21, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 21, 2009
- Product Type
- Devices
View Company Profile
ID · 450b5384-79fb-46ac-b687-bf1ec8625c45
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 557929
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Ivoclar Vivadent Manufacturing, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| October 11, 2018 | Not classified | New Jersey District Office | |
| September 20, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 22, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Ivoclar Vivadent Manufacturing, Inc.
- FDA Inspection 1121013 - 2018-10-11
- FDA Inspection 1025860 - 2017-09-20
- FDA Inspection 754045 - 2011-11-22
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