Neomedix Corporation

Form 483

Tustin, California, United StatesFEI 3003698071Issued March 29, 2018

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 3003698071.

Observations7

Issue DateMarch 29, 2018

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Neomedix Corporation
Location: Tustin, California, United States
FEI Number: 3003698071
Product Type: Devices
Issue Date: March 29, 2018
Country: United States

Inspection History, 2011 to 2019

NAI1

VAI3

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

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Neomedix Corporation FDA Form 483, Tustin, California, March 29, 2018