FDA Inspection 896205 - Intermed Group, Inc. - September 18, 2014

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Record Details

This FDA Inspection record concerns Intermed Group, Inc., with an inspection on September 18, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Intermed Group, Inc.
Inspection Date: September 18, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1258a0a7-72e1-4740-b699-d113075ce24c

Violation Codes2

21 CFR 820.20(d)21 CFR 820.22

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