FDA Inspection 999203 — Aarti Pharmalabs Limited

Aarti Pharmalabs Limited — FEI 3005256484

The FDA completed an inspection of Aarti Pharmalabs Limited on December 21, 2016 in Palghar. 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
December 21, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Palghar (India)