FDA Inspection 1050398 - Miele & Cie. KG - April 19, 2018

Record Details

This FDA Inspection record concerns Miele & Cie. KG, with an inspection on April 19, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Miele & Cie. KG
Inspection Date: April 19, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · db8ffef4-5010-4fc9-b1d7-46d57ff97f8a

Violation Codes3

21 CFR 1010.2(c)21 CFR 1030.10(c)(3)(i)21 CFR 1030.10(c)(3)(iii)

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