VertiFlex, Inc.

Form 483

Carlsbad, California, United StatesFEI 3005882106Issued July 19, 2016

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 3005882106.

Observations1

Issue DateJuly 19, 2016

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: VertiFlex, Inc.
Location: Carlsbad, California, United States
FEI Number: 3005882106
Product Type: Devices
Issue Date: July 19, 2016
Country: United States

Inspection History, 2008 to 2016

VAI4

OAI1

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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VertiFlex, Inc. FDA Form 483, Carlsbad, California, July 19, 2016