# FDA Inspection 977054 - Ivoclar Vivadent Manufacturing GmbH - June 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/ivoclar-vivadent-manufacturing-gmbh/b3937886-7e30-44fc-b4f9-0a3685339e4a
Source feed: FDA_Inspections

> FDA Inspection 977054 for Ivoclar Vivadent Manufacturing GmbH on June 23, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 977054
- Company Name: Ivoclar Vivadent Manufacturing GmbH
- Inspection Date: 2016-06-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/ivoclar-vivadent-manufacturing-gmbh/1e8d2d5a-3121-4707-9549-0c2f76e7407b

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