FDA Inspection 888696 — SK biotek

SK biotek — FEI 3009271518

The FDA completed an inspection of SK biotek on July 11, 2014 in Expo-Ro, Yuseong. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 11, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Expo-Ro, Yuseong (Korea (the Republic of))