# Ivoclar Vivadent AG – FDA Inspection, Aug 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 of Ivoclar Vivadent AG, August 24, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1130308 - 2018-09-27](https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-ag/ba0eaada-88c3-451f-a0e0-71ca8d63459b)

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