FDA Inspection 901350 - Augmenix Inc - October 17, 2014

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Record Details

This FDA Inspection record concerns Augmenix Inc, with an inspection on October 17, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Augmenix Inc
Inspection Date: October 17, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 26ec868d-6d6d-4668-8576-3cff6eb1d8aa

Violation Codes2

21 CFR 803.50(a)(1)21 CFR 820.75(a)

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