FDA Inspection 1101333 - Reprobiotech Corp - September 05, 2019

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Record Details

This FDA Inspection record concerns Reprobiotech Corp, with an inspection on September 5, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Reprobiotech Corp
Inspection Date: September 5, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e364714c-7c23-4b10-9bf7-80b1cf18040e

Violation Codes4

21 CFR 803.1721 CFR 820.20(e)21 CFR 820.50(a)(1)21 CFR 820.50(b)

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