FDA Inspection 885364 — L&K Biomed Co., Ltd.
The FDA completed an inspection of L&K Biomed Co., Ltd. on June 5, 2014 in Yongin-si. 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 5, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Yongin-si (Korea (the Republic of))