FDA Inspection 768579 — Chongqing Xinfeng Medical Instruments Co., Ltd.
The FDA completed an inspection of Chongqing Xinfeng Medical Instruments Co., Ltd. on February 17, 2012 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
- February 17, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hechuan (China)