FDA Inspection
NDX ThayerFDA 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.
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ID · fa2fdb5e-9cbf-49ab-a3c4-ac12a27ef535
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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