Westone Laboratories, Inc.

Form 483

Colorado Springs, Colorado, United StatesFEI 2094377Issued July 12, 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 2094377.

Observations11

Issue DateJuly 12, 2012

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Westone Laboratories, Inc.
Location: Colorado Springs, Colorado, United States
FEI Number: 2094377
Product Type: Devices
Issue Date: July 12, 2012
Country: United States

Inspection History, 2009 to 2017

NAI2

VAI1

OAI1

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

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Westone Laboratories, Inc. FDA Form 483, Colorado Springs, Colorado, July 12, 2012