Pharbil Waltrop Gmbh

FDA Regulatory Profile

Pharbil Waltrop Gmbh has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 6, 2025 · VAI

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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
Inspections6Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 6, 2025Waltrop, GermanyVeterinaryVoluntary Action Indicated (VAI)3004620586
Feb 7, 2024Waltrop, GermanyDrugsVoluntary Action Indicated (VAI)3004620586
Feb 14, 2020Waltrop, GermanyDrugsVoluntary Action Indicated (VAI)3004620586
Jun 22, 2018Waltrop, GermanyDrugsVoluntary Action Indicated (VAI)3004620586
Jan 24, 2014Waltrop, GermanyDrugsNo Action Indicated (NAI)3004620586
Oct 30, 2008Waltrop, GermanyDrugsVoluntary Action Indicated (VAI)3004620586

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 3004620586Waltrop, Germany6Jun 6, 2025

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