FDA Inspection 1031662 - Meluna - November 09, 2017

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Record Details

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

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

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ID · 0b8700fc-5d65-4f96-a37e-defd5aa93174

Violation Codes6

21 CFR 803.17(a)(1)21 CFR 820.100(a)21 CFR 820.18121 CFR 820.198(a)21 CFR 820.72(a)21 CFR 820.75(a)

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