Herd Mundy Richardson Limited

FDA Regulatory Profile

Herd Mundy Richardson Limited has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 10, 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
Inspections5Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 10, 2025Stockport, United KingdomDrugsVoluntary Action Indicated (VAI)3002807192
Jul 27, 2021Stockport, United KingdomDrugsVoluntary Action Indicated (VAI)3002807192
Feb 5, 2019Stockport, United KingdomDrugsVoluntary Action Indicated (VAI)3002807192
Mar 7, 2014Stockport, United KingdomDrugsNo Action Indicated (NAI)3002807192
Oct 14, 2010Stockport, United KingdomDrugsVoluntary Action Indicated (VAI)3002807192

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 3002807192Stockport, United Kingdom5Jun 10, 2025

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