# AURORA TECHNOLOGY PTE LTD – FDA Inspection, Mar 28, 2024

Source: https://www.keypedia.com/records/fda_inspections/aurora-technology-pte-ltd/bd98270f-f66e-4d55-b055-eddf2662ac56
Source feed: FDA_Inspections

> FDA inspection 1235859 of AURORA TECHNOLOGY PTE LTD, March 28, 2024. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1235859
- Company Name: AURORA TECHNOLOGY PTE LTD
- Inspection Date: 2024-03-28
- 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 Officers

- [FDA Associated Person](https://www.keypedia.com/people/daniel-j-lahar/d4e329c0-b6a5-42ca-acde-b79413b245ea)

Company: https://www.keypedia.com/companies/aurora-technology-pte-ltd/753244ad-92b0-4407-8e7d-f3574e4f778b

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