FDA Inspection 1309170 — Lepu Medical Technology (Beijing) Co., Ltd.

Lepu Medical Technology (Beijing) Co., Ltd. — FEI 3008002401

The FDA completed an inspection of Lepu Medical Technology (Beijing) Co., Ltd. on March 6, 2026 in Changping. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 6, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Changping (China)