# FDA Inspection 861149 - RANDOX TEORANTA - December 05, 2013

Source: https://www.keypedia.com/records/fda_inspections/randox-teoranta/1cdafc37-bc29-453e-ae34-e0698b5dccfd
Source feed: FDA_Inspections

> FDA Inspection 861149 for RANDOX TEORANTA on December 05, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 861149
- Company Name: RANDOX TEORANTA
- Inspection Date: 2013-12-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 861149 - 2013-12-05](https://www.keypedia.com/records/fda_inspections/randox-teoranta/a5c94850-d5b1-4149-823e-77a247085613)

Company: https://www.keypedia.com/companies/randox-teoranta/c5af8a7f-a75e-410a-88fc-fa5600771cdf

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