FDA Inspection 1089893 - EHOB, Inc. - May 06, 2019

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Record Details

This FDA Inspection record concerns EHOB, Inc., with an inspection on May 6, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: EHOB, Inc.
Inspection Date: May 6, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 85ba8d8a-67f5-47bf-857e-eeade40b05d2

Violation Codes6

21 CFR 803.1721 CFR 820.198(a)21 CFR 820.5021 CFR 820.70(a)21 CFR 820.75(a)21 CFR 820.90(b)(2)

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