FDA Inspection 1026406 - Interlectric Corporation - September 21, 2017

Record Details

This FDA Inspection record concerns Interlectric Corporation, with an inspection on September 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Interlectric Corporation
Inspection Date: September 21, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 8a67fae4-25cf-48bb-9f51-12397601e856

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.20(e)21 CFR 820.2221 CFR 820.30(a)21 CFR 820.70(b)21 CFR 820.8621 CFR 820.90(a)

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