# Ivoclar Vivadent, Inc. – FDA Inspection, Jan 11, 2018

Source: https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-inc/6edecc43-8729-40b0-9c5a-4773dd87b7fc
Source feed: FDA_Inspections

> FDA inspection 1037471 of Ivoclar Vivadent, Inc., January 11, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037471
- Company Name: Ivoclar Vivadent, Inc.
- Inspection Date: 2018-01-11
- 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: 3

## Related Documents

- FDA Inspection 836298 - 2013-06-07
- FDA Inspection 759584 - 2011-12-02
- FDA Inspection 754457 - 2011-11-16
- FDA Inspection 710802 - 2011-02-09
- FDA Inspection 650681 - 2010-03-09

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

Company: https://www.keypedia.com/companies/ivoclar-vivadent-inc/8cbf5889-296c-4161-a731-d1afeb6d0be2

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