Distribuidora La Jugosita, Inc.

FDA Regulatory Profile

Distribuidora La Jugosita, Inc. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Feb 20, 2024 · 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
Inspections8Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 20, 2024Cidra, PRFood/CosmeticsVoluntary Action Indicated (VAI)3011281553
Mar 8, 2021Cidra, PRFood/CosmeticsNo Action Indicated (NAI)3011281553
Feb 8, 2019Cidra, PRFood/CosmeticsOfficial Action Indicated (OAI)3011281553
Apr 16, 2018Cidra, PRFood/CosmeticsOfficial Action Indicated (OAI)3011281553
May 16, 2017Cidra, PRFood/CosmeticsOfficial Action Indicated (OAI)3011281553
Jan 29, 2014Cidra, PRFood/CosmeticsVoluntary Action Indicated (VAI)3011281553
Oct 6, 2011Cidra, PRFood/CosmeticsVoluntary Action Indicated (VAI)3011281553
Jul 31, 2009Cidra, PRFood/CosmeticsVoluntary Action Indicated (VAI)3011281553

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 3011281553Cidra, PR8Feb 20, 2024

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