FDA Inspection 1137122 - Orthodent Laboratory, Inc. - March 24, 2021

FDA Inspection 1137122 for Orthodent Laboratory, Inc. on March 24, 2021. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1137122 for Orthodent Laboratory, Inc. on March 24, 2021. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Orthodent Laboratory, Inc.

Inspection Date

March 24, 2021

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f9f50106-2197-4b4b-a609-329d5de1f5de

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