FDA Inspection 729744 - Mego Afek AC Ltd. - May 05, 2011

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Record Details

This FDA Inspection record concerns Mego Afek AC Ltd., with an inspection on May 5, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company: Mego Afek AC Ltd.
Inspection Date: May 5, 2011
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · edf666d7-bc1e-4aed-8bd5-55f50a85ccf9

Violation Codes2

21 CFR 820.30(g)21 CFR 820.90(a)

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