FDA Inspection 907142 - Repro Parts, Inc. - December 18, 2014

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Record Details

This FDA Inspection record concerns Repro Parts, Inc., with an inspection on December 18, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Repro Parts, Inc.
Inspection Date: December 18, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a0d8d7c3-431b-4860-b9f7-03c1a25aec56

Violation Codes2

21 CFR 803.1721 CFR 820.20(b)

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