FDA Inspection 858496 — BK Meditech Co., Ltd.
The FDA completed an inspection of BK Meditech Co., Ltd. on Nov 21, 2013 in Hwaseong. 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 21, 2013
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hwaseong (Korea (the Republic of))