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BTI Filtration

FDA Regulatory Profile

BTI Filtration has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 3, 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
Inspections5Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 3, 2025Oklahoma City, OKDevicesVoluntary Action Indicated (VAI)3003200197
May 11, 2023Oklahoma City, OKDevicesVoluntary Action Indicated (VAI)3003200197
Aug 24, 2017Oklahoma City, OKDevicesVoluntary Action Indicated (VAI)3003200197
Dec 12, 2013Oklahoma City, OKDevicesVoluntary Action Indicated (VAI)3003200197
Jan 30, 2009Oklahoma City, OKDevicesVoluntary Action Indicated (VAI)3003200197

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 3003200197Oklahoma City, OK5Dec 3, 2025

FDA data resources

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