FDA Inspection 1291134 — DM Systems Beijing Co Ltd

DM Systems Beijing Co Ltd — FEI 3008413470

The FDA completed an inspection of DM Systems Beijing Co Ltd on November 13, 2025 in Beijing. 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
November 13, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Beijing (China)