FDA Inspection 1110015 — Corentec Co., LTD

Corentec Co., LTD — FEI 3009106092

The FDA completed an inspection of Corentec Co., LTD on October 31, 2019 in Cheonan. 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
October 31, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Cheonan (Korea (the Republic of))