Illumina, Inc.

Form 483

San Diego, California, United StatesFEI 3003218906Issued August 28, 2015

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 3003218906.

Observations3

Issue DateAugust 28, 2015

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Illumina, Inc.
Location: San Diego, California, United States
FEI Number: 3003218906
Product Type: Devices
Issue Date: August 28, 2015
Country: United States

Inspection History, 2013 to 2016

NAI5

VAI2

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

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Illumina, Inc. FDA Form 483, San Diego, California, August 28, 2015