FDA Inspection 976158 - E K Industries Inc - June 02, 2016

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Record Details

This FDA Inspection record concerns E K Industries Inc, with an inspection on June 2, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: E K Industries Inc
Inspection Date: June 2, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · f116bd4f-c1e5-4646-8a64-eb13e110f815

Violation Codes2

21 CFR 820.20(c)21 CFR 820.22

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