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Delano Company, Inc.

FDA Regulatory Profile

Delano Company, Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Apr 28, 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 actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 28, 2026Grover Beach, CAFood/CosmeticsNo Action Indicated (NAI)3003303856
Feb 25, 2022Grover Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)3003303856
May 1, 2019Grover Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)3003303856
Apr 4, 2018Grover Beach, CAFood/CosmeticsOfficial Action Indicated (OAI)3003303856

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 3003303856Grover Beach, CA4Apr 28, 2026

FDA data resources

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