LumiQuick Diagnostics Inc.

Form 483

Santa Clara, California, United StatesFEI 3005984081Issued December 07, 2012

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 3005984081.

Observations7

Issue DateDecember 07, 2012

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: LumiQuick Diagnostics Inc.
Location: Santa Clara, California, United States
FEI Number: 3005984081
Product Type: Devices
Issue Date: December 07, 2012
Country: United States

Inspection History, 2012 to 2025

NAI2

VAI1

OAI2

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

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LumiQuick Diagnostics Inc. FDA Form 483, Santa Clara, California, December 7, 2012