FDA Inspection 1111038 — Guangdong Welland Technology Co.,Ltd.

Guangdong Welland Technology Co.,Ltd. — FEI 3013530241

The FDA completed an inspection of Guangdong Welland Technology Co.,Ltd. on October 31, 2019 in Zhongshan. 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
October 31, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Zhongshan (China)