FDA Inspection 918396 — Bio Focus Co. Ltd.

Bio Focus Co. Ltd. — FEI 3005841978

The FDA completed an inspection of Bio Focus Co. Ltd. on February 26, 2015 in Uiwang-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
February 26, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Uiwang-si (Korea (the Republic of))