FDA Inspection 1106208 - Deerfield Imaging, Inc. - October 01, 2019

FDA Inspection 1106208 for Deerfield Imaging, Inc. on October 01, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1106208 for Deerfield Imaging, Inc. on October 01, 2019. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 1020.30(d)(1)

21 CFR 820.100(b)

21 CFR 820.198(a)

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Record Information

Company

Deerfield Imaging, Inc.

Inspection Date

October 1, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff8600cd-29a5-4a64-97fb-1662670bae18

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