FDA Inspection 1000624 — L&K Biomed Co., Ltd.
The FDA completed an inspection of L&K Biomed Co., Ltd. on January 26, 2017 in Yongin-si. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- January 26, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Yongin-si (Korea (the Republic of))