Laax, Inc.

Form 483

Livermore, California, United StatesFEI 3008788191Issued May 22, 2015

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 3008788191.

Observations7

Issue DateMay 22, 2015

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Laax, Inc.
Location: Livermore, California, United States
FEI Number: 3008788191
Product Type: Devices
Issue Date: May 22, 2015
Country: United States

Inspection History, 2013 to 2015

NAI1

VAI1

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

Act on This Form 483

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Laax, Inc. FDA Form 483, Livermore, California, May 22, 2015