FDA Inspection 1256091 — Suzhou Kangli Orthopaedics Instrument Co., Ltd.

Suzhou Kangli Orthopaedics Instrument Co., Ltd. — FEI 3008749819

The FDA completed an inspection of Suzhou Kangli Orthopaedics Instrument Co., Ltd. on Nov 7, 2024 in Suzhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 7, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Suzhou (China)