# Ivoclar Vivadent Manufacturing GmbH – FDA Inspection, Aug 5, 2010

Source: https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-gmbh/3189a45d-d532-4567-aab9-b591faec2763
Source feed: FDA_Inspections

> FDA inspection 681145 of Ivoclar Vivadent Manufacturing GmbH, August 05, 2010. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 681145
- Company Name: Ivoclar Vivadent Manufacturing GmbH
- Inspection Date: 2010-08-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1124028 - 2018-09-06](https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-gmbh/51c11016-1c85-4e87-bd09-b99e5dca9d74)
- FDA Inspection 988687 - 2016-08-26

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