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Baker Commodities Inc

FDA Regulatory Profile

Baker Commodities Inc has 0 FDA recalls, 104 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Apr 1, 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
Inspections104Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 1, 2026West Warwick, RIVeterinaryNo Action Indicated (NAI)3004260430
Aug 4, 2025Phoenix, AZVeterinaryNo Action Indicated (NAI)2018266
Nov 29, 2023Portland, ORVeterinaryVoluntary Action Indicated (VAI)3004261063
Jun 28, 2023Vernon, CAVeterinaryNo Action Indicated (NAI)2016400
May 24, 2023Hanford, CAVeterinaryNo Action Indicated (NAI)3004333695
Feb 9, 2022East Syracuse, NYVeterinaryNo Action Indicated (NAI)3001576803
Jan 23, 2020Seattle, WAVeterinaryNo Action Indicated (NAI)3014549
Sep 5, 2019Spokane, WAVeterinaryNo Action Indicated (NAI)3002919213
Aug 13, 2019Grandview, WAVeterinaryNo Action Indicated (NAI)3004261031
Jun 25, 2019Seattle, WAVeterinaryNo Action Indicated (NAI)3014549
Jun 5, 2019Kerman, CAVeterinaryNo Action Indicated (NAI)2913791
Apr 9, 2019Vernon, CAVeterinaryNo Action Indicated (NAI)2016400
Mar 15, 2019Spokane, WAVeterinaryNo Action Indicated (NAI)3002919213
Aug 13, 2018Phoenix, AZVeterinaryNo Action Indicated (NAI)2018266
Aug 2, 2018Rochester, NYVeterinaryNo Action Indicated (NAI)1380780
Aug 1, 2018Spokane, WAVeterinaryNo Action Indicated (NAI)3002919213
May 9, 2018Grandview, WAVeterinaryNo Action Indicated (NAI)3004261031
Mar 8, 2018Vernon, CAVeterinaryNo Action Indicated (NAI)2016400
Mar 6, 2018Seattle, WAVeterinaryNo Action Indicated (NAI)3014549
Jan 17, 2018Kerman, CAVeterinaryNo Action Indicated (NAI)2913791

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 3004260430West Warwick, RI3Apr 1, 2026
FEI 2018266Phoenix, AZ11Aug 4, 2025
FEI 3004261063Portland, OR3Nov 29, 2023
FEI 2016400Vernon, CA12Jun 28, 2023
FEI 3004333695Hanford, CA3May 24, 2023
FEI 3001576803East Syracuse, NY1Feb 9, 2022
FEI 3014549Seattle, WA11Jan 23, 2020
FEI 3002919213Spokane, WA12Sep 5, 2019
FEI 3004261031Grandview, WA9Aug 13, 2019
FEI 2913791Kerman, CA11Jun 5, 2019
FEI 1380780Rochester, NY10Aug 2, 2018
FEI 3001451576Ellenburg Depot, NY1Jun 6, 2017
FEI 1317517Albany, NY4Mar 13, 2017
FEI 1213345North Billerica, MA9Feb 6, 2017
FEI 3005900403Somerton, AZ1Aug 6, 2013
FEI 3004335612Vassalboro, ME1Feb 16, 2012
FEI 3002991152Ferndale, WA2Feb 18, 2011

FDA data resources

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