# FDA Inspection 988253 - Ivoclar Vivadent AG - August 24, 2016

Source: https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-ag/82a35996-096c-44d6-9368-f7db474ac5bc
Source feed: FDA_Inspections

> FDA Inspection 988253 for Ivoclar Vivadent AG on August 24, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988253
- Company Name: Ivoclar Vivadent AG
- Inspection Date: 2016-08-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/ivoclar-vivadent-ag/7b56999b-a283-494c-bb2c-c825939bec8a

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