FDA Inspection 933478 - Groman Inc. - July 10, 2015

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Record Details

This FDA Inspection record concerns Groman Inc., with an inspection on July 10, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Groman Inc.
Inspection Date: July 10, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 72c902c6-df43-44d8-bbb2-d61ae0033c41

Violation Codes9

21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.250(b)21 CFR 820.5021 CFR 820.70(i)21 CFR 820.72(a)21 CFR 820.75(a)21 CFR 820.80(a)

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