FDA Inspection 970472 - Miele & Cie. KG - April 25, 2016

FDA Inspection 970472 for Miele & Cie. KG on April 25, 2016. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 970472 for Miele & Cie. KG on April 25, 2016. Classification: Official Action Indicated (OAI).

Violation Codes

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

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Record Information

Company

Miele & Cie. KG

Inspection Date

April 25, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fbfd3253-08b9-4dd0-b7ea-62d509ae23f2

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