FDA Inspection 1091675 — Medicore Co., Ltd.
The FDA completed an inspection of Medicore Co., Ltd. on April 25, 2019 in Seongnam. 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
- April 25, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Seongnam (Korea (the Republic of))