FDA Inspection 1235859 — AURORA TECHNOLOGY PTE LTD

AURORA TECHNOLOGY PTE LTD — FEI 3012796943

The FDA completed an inspection of AURORA TECHNOLOGY PTE LTD on Mar 28, 2024 in Singapore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 28, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Singapore (Singapore)

Citations

IDCFRDescription
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
328521 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures