# Eurolatex Sdn.Bhd. – FDA Inspection, Nov 30, 2023

Source: https://www.keypedia.com/records/fda_inspections/eurolatex-sdnbhd/bfebd843-f05b-4677-a1bb-b2cee381059c
Source feed: FDA_Inspections

> FDA inspection 1224945 of Eurolatex Sdn.Bhd., November 30, 2023. Classification: Official Action Indicated (OAI). 14 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1224945
- Company Name: Eurolatex Sdn.Bhd.
- Inspection Date: 2023-11-30
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 14

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/esteban-beltran/9a9bf6b2-ecdf-494c-82f4-5ef5932d629a)

Company: https://www.keypedia.com/companies/eurolatex-sdnbhd/722d3158-0283-4264-9355-f739fa43fabb

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