Cliantha Research Limited — Ahmedabad
USFDA inspection record for FEI 3017682080, Ahmedabad, India.
VAI
Latest classification
4
Inspections on record
0
Form 483 observations on record
History (newest first)
Inspections
17 Apr 2026
VAI — Voluntary action indicated
Bioresearch Monitoring · Drugs · FY2026
Source: FDA Data Dashboard ↗
31 May 2024
05 Apr 2024
19 Nov 2021
📎 Cite this data: Source: PharmaRoz, FDA inspection record for FEI 3017682080, updated 12 Nov 2026