LightScalpel, Inc.

Form 483

Bothell, Washington, United StatesFEI 3008720474Issued February 27, 2014

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 3008720474.

Observations7

Issue DateFebruary 27, 2014

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: LightScalpel, Inc.
Location: Bothell, Washington, United States
FEI Number: 3008720474
Product Type: Devices
Issue Date: February 27, 2014
Country: United States

Inspection History, 2012 to 2022

NAI3

VAI2

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

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LightScalpel, Inc. FDA Form 483, Bothell, Washington, February 27, 2014