FDA Inspection 848526 — SK Biotek Ireland Ltd.

SK Biotek Ireland Ltd. — FEI 3002806583

The FDA completed an inspection of SK Biotek Ireland Ltd. on September 20, 2013 in Swords. 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
September 20, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Swords (Ireland)