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Aplicare Products, LLC

FDA Regulatory Profile

Aplicare Products, LLC has 0 FDA recalls, 10 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Aug 3, 2021 · OAI

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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
Inspections10Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 3, 2021Meriden, CTDrugsOfficial Action Indicated (OAI)1220701
Sep 2, 2016Meriden, CTDrugsVoluntary Action Indicated (VAI)1220701
Jan 15, 2016Meriden, CTDrugsOfficial Action Indicated (OAI)1220701
Nov 17, 2014Meriden, CTDrugsVoluntary Action Indicated (VAI)1220701
Apr 18, 2014Meriden, CTDrugsNo Action Indicated (NAI)1220701
Sep 6, 2012Meriden, CTDrugsVoluntary Action Indicated (VAI)1220701
Nov 9, 2011Meriden, CTDrugsNo Action Indicated (NAI)1220701
Feb 4, 2011Meriden, CTDrugsVoluntary Action Indicated (VAI)1220701
Dec 17, 2009Meriden, CTDrugsVoluntary Action Indicated (VAI)1220701
Aug 7, 2009Meriden, CTFood/CosmeticsNo Action Indicated (NAI)1220701

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 1220701Meriden, CT10Aug 3, 2021

FDA data resources

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