# RANDOX TEORANTA – FDA Inspection, Dec 5, 2013

Source: https://www.keypedia.com/records/fda_inspections/randox-teoranta/a5c94850-d5b1-4149-823e-77a247085613
Source feed: FDA_Inspections

> FDA inspection 861149 of RANDOX TEORANTA, December 05, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- 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: 2

## Related Documents

- [FDA Inspection 1054635 - 2018-06-07](https://www.keypedia.com/records/fda_inspections/randox-teoranta/c0bcb1f6-9c10-4abf-87ec-482a928e9593)

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