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Creative Testing Solutions

FDA Regulatory Profile

Creative Testing Solutions has 0 FDA recalls, 62 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 4, 2026 · 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
Inspections62Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 4, 2026Charlotte, NCBiologicsNo Action Indicated (NAI)1000140241
May 18, 2026San Marcos, TXBiologicsNo Action Indicated (NAI)3009143031
Jan 14, 2026Memphis, TNBiologicsNo Action Indicated (NAI)1071905
Aug 29, 2025Tempe, AZBiologicsVoluntary Action Indicated (VAI)3000204058
Aug 1, 2024Saint Petersburg, FLBiologicsNo Action Indicated (NAI)3008082972
Sep 26, 2023Memphis, TNBiologicsNo Action Indicated (NAI)1071905
Aug 31, 2023Saint Louis, MOBiologicsNo Action Indicated (NAI)1000305305
Aug 25, 2023Bedford, TXBiologicsNo Action Indicated (NAI)3002580251
Jul 14, 2023Tempe, AZBiologicsNo Action Indicated (NAI)3000204058
Nov 3, 2022Charlotte, NCBiologicsNo Action Indicated (NAI)1000140241
Dec 10, 2021Saint Petersburg, FLBiologicsNo Action Indicated (NAI)3008082972
Aug 22, 2019Memphis, TNBiologicsNo Action Indicated (NAI)1071905
Jul 16, 2019Charlotte, NCBiologicsVoluntary Action Indicated (VAI)1000140241
Apr 16, 2019San Marcos, TXBiologicsNo Action Indicated (NAI)3009143031
Mar 21, 2019Tempe, AZBiologicsNo Action Indicated (NAI)3000204058
May 4, 2018Saint Petersburg, FLBiologicsNo Action Indicated (NAI)3008082972
Apr 26, 2018Portland, ORBiologicsNo Action Indicated (NAI)1000307460
Dec 12, 2017Bedford, TXBiologicsNo Action Indicated (NAI)3002580251
Jul 20, 2017Charlotte, NCBiologicsNo Action Indicated (NAI)1000140241
Jun 21, 2017Saint Louis, MOBiologicsNo Action Indicated (NAI)1000305305

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 1000140241Charlotte, NC10Jun 4, 2026
FEI 3009143031San Marcos, TX4May 18, 2026
FEI 1071905Memphis, TN8Jan 14, 2026
FEI 3000204058Tempe, AZ7Aug 29, 2025
FEI 3008082972Saint Petersburg, FL7Aug 1, 2024
FEI 1000305305Saint Louis, MO10Aug 31, 2023
FEI 3002580251Bedford, TX5Aug 25, 2023
FEI 1000307460Portland, OR9Apr 26, 2018
FEI 3009886096Rosemont, IL2Jan 14, 2015

FDA data resources

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