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Dhaliwal Labs South LLC

FDA Regulatory Profile

Dhaliwal Labs South LLC has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 26, 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
Inspections8Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 26, 2025Dallas, TXDrugsVoluntary Action Indicated (VAI)3007410731
Feb 7, 2023Dallas, TXVeterinaryVoluntary Action Indicated (VAI)3007410731
Apr 25, 2019Dallas, TXDrugsVoluntary Action Indicated (VAI)3007410731
Dec 20, 2017Dallas, TXDrugsVoluntary Action Indicated (VAI)3007410731
Jun 14, 2016Dallas, TXDrugsVoluntary Action Indicated (VAI)3007410731
Jun 20, 2014Dallas, TXVeterinaryVoluntary Action Indicated (VAI)3007410731
Dec 15, 2011Dallas, TXDevicesOfficial Action Indicated (OAI)3007410731
Dec 8, 2009Dallas, TXVeterinaryVoluntary Action Indicated (VAI)3007410731

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.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3007410731Dallas, TX8Jun 26, 2025

FDA data resources

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