Agilent Technologies, Inc.

Form 483

Carpinteria, California, United StatesFEI 2022180Issued October 01, 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 2022180.

Observations1

Issue DateOctober 01, 2012

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Agilent Technologies, Inc.
Location: Carpinteria, California, United States
FEI Number: 2022180
Product Type: Devices
Issue Date: October 01, 2012
Country: United States

Inspection History, 2012 to 2021

NAI4

VAI3

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

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Agilent Technologies, Inc. FDA Form 483, Carpinteria, California, October 1, 2012