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FDA Inspection
•Illumina, Inc.•November 10, 2016

Illumina, Inc. – FDA Inspection, Nov 10, 2016

Record Details

This FDA Inspection record concerns Illumina, Inc., with an inspection on November 10, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Illumina, Inc.
Inspection Date
November 10, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Kelvin Cheung (Issuing Officer)
View Company Profile

ID · bb401345-fe4c-41b7-8698-1185353966e6

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
993037
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Illumina, Inc.

11
DateClassificationOfficeProject area
June 23, 2026Not classifiedLos Angeles District Office
August 16, 2019Not classifiedLos Angeles District Office
October 5, 2017Not classifiedLos Angeles District Office
October 5, 2017Not classifiedLos Angeles District Office
December 14, 2016NAICenter for Devices and Radiological HealthBioresearch Monitoring
View all 11 other inspections on the company page
Other documents for Illumina, Inc.
  • FDA Inspection 1312600 - 2026-06-23
  • FDA Inspection 1157012 - 2019-08-16
  • FDA Inspection 1045094 - 2017-10-05
  • FDA Inspection 1045055 - 2017-10-05
  • FDA Inspection 994780 - 2016-12-14

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