# FDA Inspection 1025860 - Ivoclar Vivadent Manufacturing, Inc. - September 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-inc/92ee736c-1388-4f8c-81fd-045213887900
Source feed: FDA_Inspections

> FDA Inspection 1025860 for Ivoclar Vivadent Manufacturing, Inc. on September 20, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1025860
- Company Name: Ivoclar Vivadent Manufacturing, Inc.
- Inspection Date: 2017-09-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1025860 - 2017-09-20](https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-inc/5304c5e7-5c71-4e03-827d-d91ce4c751da)
- [FDA Inspection 754045 - 2011-11-22](https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-inc/b982b13f-2720-43b4-9c26-abf7407a4199)
- [FDA Inspection 557929 - 2009-01-21](https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-inc/0dbbaff8-1271-4409-9451-40d09454ba64)
- [FDA Inspection 557929 - 2009-01-21](https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-inc/450b5384-79fb-46ac-b687-bf1ec8625c45)

Company: https://www.keypedia.com/companies/ivoclar-vivadent-manufacturing-inc/84b0f696-b6fb-4268-b763-c6e8fa8edcaa

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7