FDA Inspection 984322 — Suzhou KD Intelligent Device Co., Ltd
The FDA completed an inspection of Suzhou KD Intelligent Device Co., Ltd on Jun 16, 2016 in Suzhou. 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 16, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Suzhou (China)