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

Open in Dashboard

ID · 66fcf092-5359-4d31-892e-f4fd2e5b0de2

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)

Full citation text and observation details available on the Dashboard.