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Macbrud Corporation

FDA Regulatory Profile

Macbrud Corporation has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Oct 20, 2026 · 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
Oct 20, 2026Miami, FLDevicesVoluntary Action Indicated (VAI)1052243
May 21, 2025Miami, FLDevicesVoluntary Action Indicated (VAI)1052243
Nov 18, 2022Miami, FLDevicesVoluntary Action Indicated (VAI)1052243
Jan 23, 2020Miami, FLDevicesNo Action Indicated (NAI)1052243
Jul 23, 2013Miami, FLDevicesVoluntary Action Indicated (VAI)1052243

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 1052243Miami, FL5Oct 20, 2026

FDA data resources

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