Creation Technologies

FDA Regulatory Profile

Creation Technologies has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Mar 9, 2023 · OAI

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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
Inspections7Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 9, 2023Mississauga, CanadaDevicesOfficial Action Indicated (OAI)3007611554
Mar 11, 2022Newark, NYDevicesNo Action Indicated (NAI)1000474105
Mar 5, 2020Burnaby, CanadaDevicesOfficial Action Indicated (OAI)3000279201
Sep 10, 2019Everett, WADevicesVoluntary Action Indicated (VAI)3004065885
Feb 14, 2019Newark, NYDevicesNo Action Indicated (NAI)1000474105
Mar 5, 2015Mississauga, CanadaDevicesVoluntary Action Indicated (VAI)3007611554
Mar 30, 2009Burnaby, CanadaDevicesVoluntary Action Indicated (VAI)3000279201

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 3007611554Mississauga, Canada2Mar 9, 2023
FEI 1000474105Newark, NY2Mar 11, 2022
FEI 3000279201Burnaby, Canada2Mar 5, 2020
FEI 3004065885Everett, WA1Sep 10, 2019

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