FDA Inspection 1004196 - Oakworks Inc - March 16, 2017

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Record Details

This FDA Inspection record concerns Oakworks Inc, with an inspection on March 16, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Oakworks Inc
Inspection Date: March 16, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 93847536-5665-4d72-98fa-65283e0b5902

Violation Codes10

21 CFR 803.50(a)(2)21 CFR 806.10(a)(1)21 CFR 820.100(b)21 CFR 820.18421 CFR 820.198(c)21 CFR 820.20(c)21 CFR 820.250(b)21 CFR 820.30(f)21 CFR 820.80(d)21 CFR 820.90(a)

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