FDA Inspection 1071189 - WEBER MEDICAL GMBH - November 08, 2018

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Record Details

This FDA Inspection record concerns WEBER MEDICAL GMBH, with an inspection on November 8, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: WEBER MEDICAL GMBH
Inspection Date: November 8, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9e51c108-6328-4884-a819-5c97963b1a0e

Violation Codes10

21 CFR 1002.1321 CFR 1010.2(b)21 CFR 1040.10(f)(5)(ii)21 CFR 1040.10(h)(1)(iii)21 CFR 1040.10(h)(1)(iv)21 CFR 1040.10(h)(2)(i)21 CFR 1040.11(a)(3)21 CFR 803.17(a)(3)21 CFR 806.20(b)(4)21 CFR 820.100(a)

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