Cliantha Research Limited

FDA Regulatory Profile

Cliantha Research Limited has 0 FDA recalls, 15 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Cliantha Research Limited" and its spelling variant "Cliantha Research".

Latest inspection
Apr 17, 2026 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections15Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Cliantha Research Limited's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Cliantha Research Limited: FDA inspections per year 2017: 0 inspections020172018: 3 inspections320182019: 3 inspections320192020: 0 inspections020202021: 1 inspections120212022: 2 inspections220222023: 1 inspections120232024: 4 inspections420242025: 0 inspections020252026: 1 inspections12026
YearInspectionsOAIWarning lettersRecall recordsClass I
202610000
202500000
202440000
202310000
202220000
202110000
202000000
201930000
201830000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

15 inspections from Mar 9, 2018 to Apr 17, 2026.

DateSiteProductClassificationFEI
Apr 17, 2026Ahmedabad, IndiaDrugsVoluntary Action Indicated (VAI)3017682080
May 31, 2024Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3017682080
Apr 26, 2024Noida, IndiaDrugsNo Action Indicated (NAI)3030708916
Apr 12, 2024Vadodara, IndiaDrugsNo Action Indicated (NAI)3007078964
Apr 5, 2024Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3017682080
Nov 3, 2023Noida, IndiaDrugsNo Action Indicated (NAI)3013167427
Nov 10, 2022Mississauga, CanadaDrugsNo Action Indicated (NAI)3011341889
Jul 8, 2022Vadodara, IndiaDrugsNo Action Indicated (NAI)3007078964
Nov 19, 2021Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3017682080
Dec 6, 2019Ahmedabad, IndiaDrugsVoluntary Action Indicated (VAI)3009853705
Jul 19, 2019Vadodara, IndiaDrugsNo Action Indicated (NAI)3007078964
Jul 19, 2019Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3005821331
Nov 2, 2018Mississauga, CanadaDrugsNo Action Indicated (NAI)3011341889
Aug 3, 2018Ahmedabad, IndiaDrugsNo Action Indicated (NAI)3005821331
Mar 9, 2018Noida, IndiaDrugsNo Action Indicated (NAI)3013167427
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

7 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3017682080Ahmedabad, India4Apr 17, 2026
FEI 3030708916Noida, India1Apr 26, 2024
FEI 3007078964Vadodara, India3Apr 12, 2024
FEI 3013167427Noida, India2Nov 3, 2023
FEI 3011341889Mississauga, Canada2Nov 10, 2022
FEI 3009853705Ahmedabad, India1Dec 6, 2019
FEI 3005821331Ahmedabad, India2Jul 19, 2019

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.