# FDA Inspection 969543 - RANDOX LABORATORIES, LTD. - April 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/randox-laboratories-ltd/bf726872-8069-4965-968b-41e9406c4d49
Source feed: FDA_Inspections

> FDA Inspection 969543 for RANDOX LABORATORIES, LTD. on April 28, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 969543
- Company Name: RANDOX LABORATORIES, LTD.
- 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-ltd/1296ae89-c0c5-4938-b181-f602f24fb17e

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