FDA Inspection 939517 - The Morel Company, LLC - August 27, 2015

FDA Inspection 939517 for The Morel Company, LLC on August 27, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 939517 for The Morel Company, LLC on August 27, 2015. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.100(a)

21 CFR 820.30(i)

21 CFR 820.90(b)(2)

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Record Information

Company

The Morel Company, LLC

Inspection Date

August 27, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 5d96fe83-def3-4333-89d0-3057d8bc9a1d

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