United Metal Fabricators Inc

FDA Regulatory Profile

United Metal Fabricators Inc has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 12, 2025 · 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
Inspections6Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 12, 2025Johnstown, PADevicesNo Action Indicated (NAI)2518399
Apr 27, 2017Johnstown, PADevicesVoluntary Action Indicated (VAI)2518399
Jun 27, 2013Johnstown, PADevicesNo Action Indicated (NAI)2518399
Aug 8, 2011Johnstown, PADevicesNo Action Indicated (NAI)2518399
Apr 21, 2011Johnstown, PADevicesVoluntary Action Indicated (VAI)2518399
Oct 17, 2008Johnstown, PADevicesVoluntary Action Indicated (VAI)2518399

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 2518399Johnstown, PA6Aug 12, 2025

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