Neopharm Labs Inc.

FDA Regulatory Profile

Neopharm Labs Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 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 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 12, 2025Blainville, CanadaDrugsNo Action Indicated (NAI)3002807703
Mar 19, 2019Blainville, CanadaDrugsNo Action Indicated (NAI)3002807703
Feb 9, 2018Blainville, CanadaDrugsNo Action Indicated (NAI)3002807703
Nov 14, 2014Blainville, CanadaDrugsNo Action Indicated (NAI)3002807703
May 1, 2012Blainville, CanadaDrugsNo Action Indicated (NAI)3002807703
Feb 16, 2010Blainville, CanadaDrugsNo Action Indicated (NAI)3002807703

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 3002807703Blainville, Canada6Sep 12, 2025

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