FDA Inspection 1236751 — SK Biotek Co., Ltd. (Sejong Plant)

SK Biotek Co., Ltd. (Sejong Plant) — FEI 3014286622

The FDA completed an inspection of SK Biotek Co., Ltd. (Sejong Plant) on Mar 22, 2024 in Sejong. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 22, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sejong (Korea (the Republic of))