Spine Wave, Inc.

Form 483

Shelton, Connecticut, United StatesFEI 3004638600Issued January 10, 2017

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 3004638600.

Observations2

Issue DateJanuary 10, 2017

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Spine Wave, Inc.
Location: Shelton, Connecticut, United States
FEI Number: 3004638600
Product Type: Devices
Issue Date: January 10, 2017
Country: United States

Inspection History, 2009 to 2026

NAI4

VAI1

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

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Spine Wave, Inc. FDA Form 483, Shelton, Connecticut, January 10, 2017