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Producto La Samaritana, Inc.

FDA Regulatory Profile

Producto La Samaritana, Inc. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 25, 2026 · 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
Inspections3Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 25, 2026San Lorenzo, PRFood/CosmeticsVoluntary Action Indicated (VAI)3010899218
Apr 19, 2023San Lorenzo, PRFood/CosmeticsVoluntary Action Indicated (VAI)3010899218
Sep 13, 2019San Lorenzo, PRFood/CosmeticsVoluntary Action Indicated (VAI)3010899218

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 3010899218San Lorenzo, PR3Sep 25, 2026

FDA data resources

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