Wuxi Medical lnstrument Factory Co., Ltd.

FDA Regulatory Profile

Wuxi Medical lnstrument Factory Co., Ltd. appears in FDA public data with 1 recall, 0 510(k) clearances, 2 FDA inspections, and 2 compliance actions on record. Its most recent recall (D-0247-2025, Class II) was initiated on February 12, 2025.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
2
Compliance Actions
2

Recent Recalls

NumberClassProductDate
D-0247-2025Class IIViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100 pieces per Box,February 12, 2025