FDA Inspection 967552 — Zydus Lifesciences Limited

Zydus Lifesciences Limited — FEI 3006026405

The FDA completed an inspection of Zydus Lifesciences Limited on March 18, 2016 in Ahmedabad. 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
March 18, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ahmedabad (India)