FDA Inspection 1040691 - NDX Thayer - February 01, 2018

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Record Details

This FDA Inspection record concerns NDX Thayer, with an inspection on February 1, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: NDX Thayer
Inspection Date: February 1, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b04303d1-a8fa-45a6-81fc-a88994dba010

Violation Codes8

21 CFR 820.12021 CFR 820.18121 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.72(a)21 CFR 820.80(d)

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