FDA Inspection 1028487 — Chongqing Xinfeng Medical Instruments Co., Ltd.
The FDA completed an inspection of Chongqing Xinfeng Medical Instruments Co., Ltd. on September 14, 2017 in Hechuan. 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
- September 14, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Hechuan (China)