Kindeva Drug Delivery L.P. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Kindeva Drug Delivery L.P. has 0 FDA recalls, 20 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Kindeva Drug Delivery L.P." is on file.

What these totals cover: FDA records filed under the name "Kindeva Drug Delivery L.P." and its spelling variants "Kindeva Drug Delivery L.P", "Kindeva Drug Delivery Limited".

Latest inspection
Nov 13, 2025 · 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
Inspections20Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Kindeva Drug Delivery L.P.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Kindeva Drug Delivery L.P.: FDA inspections per year 2017: 2 inspections220172018: 1 inspections120182019: 2 inspections220192020: 0 inspections020202021: 2 inspections220212022: 0 inspections020222023: 0 inspections020232024: 0 inspections020242025: 2 inspections220252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202520000
202400000
202300000
202200000
202120000
202000000
201920000
201810000
201720000

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

20 inspections from Feb 2, 2009 to Nov 13, 2025.

DateSiteProductClassificationFEI
Nov 13, 2025Northridge, CADrugsVoluntary Action Indicated (VAI)2010441
Mar 14, 2025Loughborough, United KingdomDrugsVoluntary Action Indicated (VAI)3002807586
Jul 28, 2021Northridge, CADrugsNo Action Indicated (NAI)2010441
May 27, 2021Loughborough, United KingdomDrugsVoluntary Action Indicated (VAI)3002807586
Jan 25, 2019Northridge, CADrugsVoluntary Action Indicated (VAI)2010441
Jan 25, 2019Northridge, CADrugsNo Action Indicated (NAI)2010441
May 3, 2018Loughborough, United KingdomDrugsVoluntary Action Indicated (VAI)3002807586
Jun 30, 2017Loughborough, United KingdomDrugsVoluntary Action Indicated (VAI)3002807586
Mar 6, 2017Northridge, CADrugsVoluntary Action Indicated (VAI)2010441
Aug 12, 2016Loughborough, United KingdomDrugsVoluntary Action Indicated (VAI)3002807586
Sep 1, 2015Northridge, CADrugsVoluntary Action Indicated (VAI)2010441
Mar 5, 2015Loughborough, United KingdomDrugsNo Action Indicated (NAI)3002807586
Sep 17, 2014Northridge, CADrugsVoluntary Action Indicated (VAI)2010441
Aug 23, 2013Northridge, CADrugsNo Action Indicated (NAI)2010441
Apr 15, 2013Loughborough, United KingdomDrugsVoluntary Action Indicated (VAI)3002807586
Jan 4, 2012Northridge, CADrugsVoluntary Action Indicated (VAI)2010441
Nov 5, 2010Northridge, CADrugsNo Action Indicated (NAI)2010441
Feb 12, 2010Northridge, CADrugsVoluntary Action Indicated (VAI)2010441
Apr 17, 2009Loughborough, United KingdomDrugsVoluntary Action Indicated (VAI)3002807586
Feb 2, 2009Northridge, CADrugsVoluntary Action Indicated (VAI)2010441
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

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 2010441Northridge, CA12Nov 13, 2025
FEI 3002807586Loughborough, United Kingdom8Mar 14, 2025

Kindeva Drug Delivery L.P. and the FDA: common questions

Has Kindeva Drug Delivery L.P. received an FDA warning letter?

No FDA warning letter addressed to the name "Kindeva Drug Delivery L.P." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Kindeva Drug Delivery L.P. received an FDA Form 483?

FDA has not published a Form 483 for "Kindeva Drug Delivery L.P." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Kindeva Drug Delivery L.P.?

The most recent FDA inspection on file ended Nov 13, 2025 at Northridge, CA and was classified VAI. FDA has 20 inspections of Kindeva Drug Delivery L.P. on file.

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