FDA Inspection 1069071 — Mediana Co., Ltd.
The FDA completed an inspection of Mediana Co., Ltd. on Sep 6, 2018 in Wonju. 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)
- End Date
- Sep 6, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Wonju (Korea (the Republic of))