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Mayer Bros. Apple Products, Inc.

FDA Regulatory Profile

Mayer Bros. Apple Products, Inc. has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 3, 2026 · 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
Inspections7Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 3, 2026Barker, NYFood/CosmeticsNo Action Indicated (NAI)1315843
May 16, 2025Buffalo, NYFood/CosmeticsVoluntary Action Indicated (VAI)1312291
Nov 22, 2021Buffalo, NYFood/CosmeticsNo Action Indicated (NAI)1312291
Nov 23, 2010Buffalo, NYFood/CosmeticsNo Action Indicated (NAI)1312291
May 26, 2009Barker, NYFood/CosmeticsNo Action Indicated (NAI)1315843
Mar 24, 2009Barker, NYFood/CosmeticsNo Action Indicated (NAI)1315843
Feb 19, 2009Buffalo, NYFood/CosmeticsNo Action Indicated (NAI)1312291

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 1315843Barker, NY3Jun 3, 2026
FEI 1312291Buffalo, NY4May 16, 2025

FDA data resources

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