FDA Inspection 1025048 - Hydrofera, LLC - August 23, 2017

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Record Details

This FDA Inspection record concerns Hydrofera, LLC, with an inspection on August 23, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Hydrofera, LLC
Inspection Date: August 23, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 02603b43-c064-4841-81c5-24b4aaf7cb7d

Violation Codes2

21 CFR 820.30(i)21 CFR 820.72(a)

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