FDA Inspection 948867 — Famidoc Technology Co., Ltd.
The FDA completed an inspection of Famidoc Technology Co., Ltd. on Nov 5, 2015 in Dongguan. 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
- Nov 5, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Dongguan (China)