FDA Inspection 837793 - Mani, Inc. - Kiyohara Facility - May 23, 2013

Record Details

This FDA Inspection record concerns Mani, Inc. - Kiyohara Facility, with an inspection on May 23, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Mani, Inc. - Kiyohara Facility
Inspection Date: May 23, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 64a10875-1a3a-4d4d-ae34-8538a087cfb9

Violation Codes3

21 CFR 820.100(b)21 CFR 820.198(a)21 CFR 820.30(c)

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