FDA Inspection 1112024 — Kyongbo Pharmaceutical Co., Ltd.

Kyongbo Pharmaceutical Co., Ltd. — FEI 3003773799

The FDA completed an inspection of Kyongbo Pharmaceutical Co., Ltd. on December 6, 2019 in Asan. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 6, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Asan (Korea (the Republic of))