FDA Inspection 1319806 — Cliantha Research Limited

Cliantha Research Limited — FEI 3017682080

The FDA completed an inspection of Cliantha Research Limited on April 17, 2026 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
April 17, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Ahmedabad (India)

Additional Details

Bioanalytical BA/BE