FDA Inspection 1098820 — Ajanta Pharma Limited

Ajanta Pharma Limited — FEI 3012664809

The FDA completed an inspection of Ajanta Pharma Limited on June 22, 2019 in Bharuch. 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
June 22, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bharuch (India)