# Ivoclar Vivadent Manufacturing, Inc. – FDA Inspection, Jan 21, 2009

Source: https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-inc/450b5384-79fb-46ac-b687-bf1ec8625c45
Source feed: FDA_Inspections

> FDA inspection 557929 of Ivoclar Vivadent Manufacturing, Inc., January 21, 2009. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 557929
- Company Name: Ivoclar Vivadent Manufacturing, Inc.
- Inspection Date: 2009-01-21
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1121013 - 2018-10-11
- [FDA Inspection 1025860 - 2017-09-20](https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-inc/92ee736c-1388-4f8c-81fd-045213887900)
- FDA Inspection 754045 - 2011-11-22

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