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Nucro-Technics, Inc.

FDA Regulatory Profile

Nucro-Technics, Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 20, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections6Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 20, 2025Scarborough, CanadaDrugsVoluntary Action Indicated (VAI)3002807768
Dec 4, 2018Scarborough, CanadaDrugsVoluntary Action Indicated (VAI)3002807768
Dec 14, 2016Scarborough, CanadaDrugsNo Action Indicated (NAI)3002807768
Dec 13, 2013Scarborough, CanadaDrugsNo Action Indicated (NAI)3002807768
Sep 11, 2013Scarborough, CanadaDrugsVoluntary Action Indicated (VAI)3002807768
Jan 28, 2010Scarborough, CanadaDrugsNo Action Indicated (NAI)3002807768

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 3002807768Scarborough, Canada6May 20, 2025

FDA data resources

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