FDA Inspection 548500 — Scinopharm Taiwan, Ltd.

Scinopharm Taiwan, Ltd. — FEI 3002840477

The FDA completed an inspection of Scinopharm Taiwan, Ltd. on October 23, 2008 in Tainan City. 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
October 23, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tainan City (Taiwan)