FDA Inspection 979022 - Netech Corp. - June 16, 2016

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Record Details

This FDA Inspection record concerns Netech Corp., with an inspection on June 16, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Netech Corp.
Inspection Date: June 16, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5bb2e16b-cc53-4d54-ad6c-e12c1dab4910

Violation Codes2

21 CFR 820.100(a)21 CFR 820.30(i)

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