Campolor, Inc.

FDA Regulatory Profile

Campolor, Inc. has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Aug 30, 2024 · NAI

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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
Inspections7Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 30, 2024Ponce, PRFood/CosmeticsNo Action Indicated (NAI)3009412997
Jun 17, 2021Ponce, PRFood/CosmeticsVoluntary Action Indicated (VAI)3009412997
Sep 21, 2018Ponce, PRFood/CosmeticsOfficial Action Indicated (OAI)3009412997
Dec 20, 2017Ponce, PRFood/CosmeticsVoluntary Action Indicated (VAI)3009412997
Aug 22, 2016Ponce, PRFood/CosmeticsVoluntary Action Indicated (VAI)3009412997
Jul 6, 2011Ponce, PRFood/CosmeticsVoluntary Action Indicated (VAI)3009412997
Dec 29, 2009Ponce, PRFood/CosmeticsVoluntary Action Indicated (VAI)3009412997

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 3009412997Ponce, PR7Aug 30, 2024

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