FDA Inspection 1014538 - Orion Vision Group - March 29, 2017

FDA Inspection 1014538 for Orion Vision Group on March 29, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1014538 for Orion Vision Group on March 29, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Orion Vision Group

Inspection Date

March 29, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fbf228a9-f0b6-43d7-8099-464ec575367a

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