# FDA Inspection 969542 - Randox Laboratories, Limited - April 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/randox-laboratories-limited/4fe2b409-5e0a-4615-8336-6b5e2f56d44e
Source feed: FDA_Inspections

> FDA Inspection 969542 for Randox Laboratories, Limited on April 28, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 969542
- Company Name: Randox Laboratories, Limited
- Inspection Date: 2016-04-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/randox-laboratories-limited/ae95c254-5113-41df-bfd7-d9f29e584dc0

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