FDA Inspection 1027744 — Dragon Heart Medical Devices Co., Ltd.
The FDA completed an inspection of Dragon Heart Medical Devices Co., Ltd. on July 21, 2017 in Kaiping. 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
- July 21, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Kaiping (China)