FDA Inspection 1040691 - NDX Thayer - February 01, 2018

FDA Inspection 1040691 for NDX Thayer on February 01, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1040691 for NDX Thayer on February 01, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.120

21 CFR 820.181

21 CFR 820.198(a)

21 CFR 820.20(c)

21 CFR 820.22

21 CFR 820.25(b)

21 CFR 820.72(a)

21 CFR 820.80(d)

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Record Information

Company

NDX Thayer

Inspection Date

February 1, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa2fdb5e-9cbf-49ab-a3c4-ac12a27ef535

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