FDA Inspection 1097061 — Ajanta Pharma Ltd.

Ajanta Pharma Ltd. — FEI 3006785788

The FDA completed an inspection of Ajanta Pharma Ltd. on June 28, 2019 in Paithan. 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 28, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Paithan (India)