FDA Inspection 1243900 — AI DE Diagnostic Co., Ltd

AI DE Diagnostic Co., Ltd — FEI 3008760472

The FDA completed an inspection of AI DE Diagnostic Co., Ltd on May 30, 2024 in Qingdao. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 30, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Qingdao (China)