# Illumina, Inc. – FDA Inspection, Aug 28, 2015

Source: https://www.keypedia.com/records/fda_inspections/illumina-inc/ac0cf899-6931-489d-b7eb-b849872b8dd0
Source feed: FDA_Inspections

> FDA inspection 941363 of Illumina, Inc., August 28, 2015. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 11 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 941363
- Company Name: Illumina, Inc.
- Inspection Date: 2015-08-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1312600 - 2026-06-23
- [FDA Inspection 1157012 - 2019-08-16](https://www.keypedia.com/records/fda_inspections/illumina-inc/d084b018-9ca8-43e1-995a-ea1abacae382)
- [FDA Inspection 1045094 - 2017-10-05](https://www.keypedia.com/records/fda_inspections/illumina-inc/8628d4c6-7095-43c7-825c-cea3210db35b)
- [FDA Inspection 1045055 - 2017-10-05](https://www.keypedia.com/records/fda_inspections/illumina-inc/5a80de91-5d0c-452b-a5c9-406cb652f030)
- FDA Inspection 994780 - 2016-12-14

Company: https://www.keypedia.com/companies/illumina-inc/6c2f2a3d-e3f1-4f43-b2b6-34ec89cbd76b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7