FDA Inspection 1083809 — Daewoo Pharmaceutical Co., Ltd.

Daewoo Pharmaceutical Co., Ltd. — FEI 1000448124

The FDA completed an inspection of Daewoo Pharmaceutical Co., Ltd. on February 22, 2019 in Saha. 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
February 22, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saha (Korea (the Republic of))