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Argenta Dundee Limited

FDA Regulatory Profile

Argenta Dundee Limited has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 5, 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
Inspections6Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 5, 2025Dundee, United KingdomDrugsVoluntary Action Indicated (VAI)3002792064
Jan 20, 2022Dundee, United KingdomVeterinaryVoluntary Action Indicated (VAI)3002792064
Jun 28, 2018Dundee, United KingdomVeterinaryNo Action Indicated (NAI)3002792064
Apr 22, 2016Dundee, United KingdomVeterinaryNo Action Indicated (NAI)3002792064
Jan 24, 2013Dundee, United KingdomVeterinaryVoluntary Action Indicated (VAI)3002792064
Aug 4, 2009Dundee, United KingdomDrugsVoluntary Action Indicated (VAI)3002792064

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 3002792064Dundee, United Kingdom6Jun 5, 2025

FDA data resources

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