KBD, Inc.

Form 483

North Las Vegas, Nevada, United StatesFEI 1022129Issued December 23, 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 1022129.

Observations1

Issue DateDecember 23, 2016

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: KBD, Inc.
Location: North Las Vegas, Nevada, United States
FEI Number: 1022129
Product Type: Devices
Issue Date: December 23, 2016
Country: United States

Inspection History, 2011 to 2019

VAI3

OAI1

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

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KBD, Inc. FDA Form 483, North Las Vegas, Nevada, December 23, 2016