FDA Inspection 1016239 — IDT Electronics (Shenzhen) Co., Ltd.
The FDA completed an inspection of IDT Electronics (Shenzhen) Co., Ltd. on June 1, 2017 in Shenzhen. 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
- June 1, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Shenzhen (China)