FDA Inspection 953454 — Uzinmedicare Co.

Uzinmedicare Co. — FEI 3008604531

The FDA completed an inspection of Uzinmedicare Co. on Dec 10, 2015 in Sungnam Si. 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
Dec 10, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Sungnam Si (Korea (the Republic of))