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Dr. Reddy's Laboratories (EU) Ltd.

FDA Regulatory Profile

Dr. Reddy's Laboratories (EU) Ltd. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 5, 2025 · VAI

Newer recall under related name Reddy Laboratories: Nov 11, 2025, D-0219-2026.

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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
Inspections3Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Reddy Laboratories
Same company group		1640281Nov 11, 2025 (D-0219-2026)
Reddy Laboratories New York
Same company group		0030—
Reddy Laboratories Lmtd
Same company group		0010—

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 5, 2025Mirfield, United KingdomDrugsVoluntary Action Indicated (VAI)3002807544
Oct 24, 2019Mirfield, United KingdomDrugsVoluntary Action Indicated (VAI)3002807544
Dec 20, 2013Mirfield, United KingdomDrugsNo Action Indicated (NAI)3002807544

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means 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

FacilityLocationInspectionsLatest
FEI 3002807544Mirfield, United Kingdom3Sep 5, 2025

FDA data resources

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