FDA Inspection 1031232 - AMYLIOR INC. - November 09, 2017

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Record Details

This FDA Inspection record concerns AMYLIOR INC., with an inspection on November 9, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: AMYLIOR INC.
Inspection Date: November 9, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · f30d151e-3ee9-41a6-b2c5-5a00250950b2

Violation Codes6

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.198(c)21 CFR 820.30(a)21 CFR 820.90(a)

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