Bell International Laboratories, Inc.

FDA Regulatory Profile

Bell International Laboratories, Inc. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jun 12, 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
Inspections8Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 12, 2025Eagan, MNDrugsVoluntary Action Indicated (VAI)3005574978
Sep 19, 2023Eagan, MNDrugsOfficial Action Indicated (OAI)3005574978
Jun 22, 2017Eagan, MNDrugsVoluntary Action Indicated (VAI)3005574978
Jan 29, 2015Eagan, MNDrugsVoluntary Action Indicated (VAI)3005574978
May 14, 2014Eagan, MNDrugsNo Action Indicated (NAI)3005574978
Jun 26, 2013Eagan, MNDevicesVoluntary Action Indicated (VAI)3005574978
Nov 9, 2010Eagan, MNDrugsVoluntary Action Indicated (VAI)3005574978
Jul 7, 2009Eagan, MNDrugsVoluntary Action Indicated (VAI)3005574978

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 3005574978Eagan, MN8Jun 12, 2025

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