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Calapaz Corp.

FDA Regulatory Profile

Calapaz Corp. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 26, 2026 · 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
Inspections4Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 26, 2026Bronx, NYFood/CosmeticsNo Action Indicated (NAI)3011212485
Jul 1, 2022Bronx, NYFood/CosmeticsOfficial Action Indicated (OAI)3011212485
Dec 4, 2020Bronx, NYFood/CosmeticsVoluntary Action Indicated (VAI)3011212485
Aug 16, 2018Bronx, NYFood/CosmeticsVoluntary Action Indicated (VAI)3011212485

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 3011212485Bronx, NY4May 26, 2026

FDA data resources

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