Mani, Inc. - Kiyohara Facility

Form 483

Utsunomiya, -, JapanFEI 3002692886Issued May 23, 2013

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3002692886.

Observations3

Issue DateMay 23, 2013

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Mani, Inc. - Kiyohara Facility
Location: Utsunomiya, -, Japan
FEI Number: 3002692886
Product Type: Devices
Issue Date: May 23, 2013
Country: Japan

Inspection History, 2010 to 2018

NAI1

VAI2

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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Mani, Inc. - Kiyohara Facility FDA Form 483, Utsunomiya, May 23, 2013