XF Enterprises Inc

FDA Regulatory Profile

XF Enterprises Inc has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 2, 2025 · VAI

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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
Inspections7Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 2, 2025East Earl, PAVeterinaryVoluntary Action Indicated (VAI)2514348
Jan 17, 2024Pratt, KSVeterinaryVoluntary Action Indicated (VAI)1921258
Nov 3, 2016Pratt, KSVeterinaryVoluntary Action Indicated (VAI)1921258
Jan 29, 2016Pratt, KSVeterinaryOfficial Action Indicated (OAI)1921258
Mar 19, 2012Pratt, KSVeterinaryNo Action Indicated (NAI)1921258
Mar 15, 2012East Earl, PAVeterinaryVoluntary Action Indicated (VAI)2514348
Jun 24, 2011Pratt, KSVeterinaryVoluntary Action Indicated (VAI)1921258

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 2514348East Earl, PA2Jul 2, 2025
FEI 1921258Pratt, KS5Jan 17, 2024

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