FDA Inspection 978118 — Tonglu Medical Instrument Co. Ltd.
The FDA completed an inspection of Tonglu Medical Instrument Co. Ltd. on Jun 2, 2016 in Hangzhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 2, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Hangzhou (China)