FDA Inspection 753353 — Alivus Life Sciences Limited

Alivus Life Sciences Limited — FEI 3004006229

The FDA completed an inspection of Alivus Life Sciences Limited on October 15, 2011 in Ankleshwar. 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 15, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ankleshwar (India)