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Unette Corp

FDA Regulatory Profile

Unette Corp has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 11, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections6Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 11, 2025Randolph, NJDrugsVoluntary Action Indicated (VAI)2210679
Jun 22, 2022Randolph, NJDrugsNo Action Indicated (NAI)2210679
Dec 28, 2016Randolph, NJDrugsNo Action Indicated (NAI)2210679
Jul 16, 2014Randolph, NJDrugsNo Action Indicated (NAI)2210679
Feb 15, 2012Randolph, NJDrugsVoluntary Action Indicated (VAI)2210679
Dec 30, 2009Randolph, NJDrugsVoluntary Action Indicated (VAI)2210679

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 2210679Randolph, NJ6Sep 11, 2025

FDA data resources

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