FDA Inspection 1242757 — Hangzhou Jimushi Meditech Co., Ltd

Hangzhou Jimushi Meditech Co., Ltd — FEI 3016863553

The FDA completed an inspection of Hangzhou Jimushi Meditech Co., Ltd on May 23, 2024 in Hangzhou. 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
May 23, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Hangzhou (China)