FDA Inspection 1067061 - Myerson LLC - September 28, 2018

FDA Inspection 1067061 for Myerson LLC on September 28, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1067061 for Myerson LLC on September 28, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.30(i)

21 CFR 820.80(b)

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Record Information

Company

Myerson LLC

Inspection Date

September 28, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa306510-2edc-4593-9d37-a3127e8e7334

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