# RANDOX TEORANTA – FDA Inspection, Jun 7, 2018

Source: https://www.keypedia.com/records/fda_inspections/randox-teoranta/c0bcb1f6-9c10-4abf-87ec-482a928e9593
Source feed: FDA_Inspections

> FDA inspection 1054635 of RANDOX TEORANTA, June 07, 2018. 4 citations under 21 CFR parts 820 and 1002. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1054635
- Company Name: RANDOX TEORANTA
- Inspection Date: 2018-06-07
- Project Area: Postmarket Assurance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 4

## Related Documents

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

## Related Officers

- Issuing Officer

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

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8