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Zeigler Brothers, Inc.

FDA Regulatory Profile

Zeigler Brothers, Inc. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jan 22, 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
Inspections3Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 22, 2026Gardners, PAVeterinaryNo Action Indicated (NAI)2511318
Aug 20, 2025East Berlin, PAVeterinaryVoluntary Action Indicated (VAI)2550021
Apr 6, 2022East Berlin, PAVeterinaryNo Action Indicated (NAI)2550021

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 2511318Gardners, PA1Jan 22, 2026
FEI 2550021East Berlin, PA2Aug 20, 2025

FDA data resources

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