FDA Inspection 780529 — SHENZHEN KINGYIELD TECHNOLOGY CO., LTD
The FDA completed an inspection of SHENZHEN KINGYIELD TECHNOLOGY CO., LTD on May 4, 2012 in Shenzhen China. 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
- May 4, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Shenzhen China (China)