FDA Inspection 695735 - Mani, Inc. - Kiyohara Facility - October 07, 2010

Record Details

This FDA Inspection record concerns Mani, Inc. - Kiyohara Facility, with an inspection on October 7, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Mani, Inc. - Kiyohara Facility
Inspection Date: October 7, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 805ed79b-2d18-4bfd-a01c-71ac1b8a2832

Violation Codes5

21 CFR 820.100(b)21 CFR 820.198(a)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.250(b)

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