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Nene El Pescador, Inc.

FDA Regulatory Profile

Nene El Pescador, Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 5, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections4Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 5, 2025Chula Vista, CAFood/CosmeticsNo Action Indicated (NAI)3013984251
Aug 4, 2022Chula Vista, CAFood/CosmeticsVoluntary Action Indicated (VAI)3013984251
Aug 19, 2021Chula Vista, CAFood/CosmeticsVoluntary Action Indicated (VAI)3013984251
Oct 5, 2018Chula Vista, CAFood/CosmeticsVoluntary Action Indicated (VAI)3013984251

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 3013984251Chula Vista, CA4Jun 5, 2025

FDA data resources

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