# FDA Inspection 681145 - Ivoclar Vivadent Manufacturing GmbH - August 05, 2010

Source: https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-gmbh/0c25cc53-d485-4046-96c9-40342d88cd5b
Source feed: FDA_Inspections

> FDA Inspection 681145 for Ivoclar Vivadent Manufacturing GmbH on August 05, 2010. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 681145
- Company Name: Ivoclar Vivadent Manufacturing GmbH
- Inspection Date: 2010-08-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 988687 - 2016-08-26](https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-gmbh/997cb0d9-44a6-440a-ab9a-adc4566a7203)
- [FDA Inspection 681145 - 2010-08-05](https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-gmbh/3189a45d-d532-4567-aab9-b591faec2763)

Company: https://www.keypedia.com/companies/ivoclar-vivadent-manufacturing-gmbh/0c03d131-9542-41ee-9f11-aeffe1061fe3

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