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Sunshine Mills, Inc.

FDA Regulatory Profile

Sunshine Mills, Inc. has 0 FDA recalls, 21 inspections, 0 510(k) clearances and 2 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
Inspections21Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 4, 2026Tupelo, MSVeterinaryNo Action Indicated (NAI)1018573
May 22, 2026Red Bay, ALVeterinaryVoluntary Action Indicated (VAI)1024376
May 6, 2026Dublin, GAVeterinaryNo Action Indicated (NAI)3003273225
Dec 4, 2025Red Bay, ALVeterinaryVoluntary Action Indicated (VAI)1024376
Feb 6, 2025Joplin, MOVeterinaryNo Action Indicated (NAI)3003658370
Jun 13, 2024Red Bay, ALVeterinaryNo Action Indicated (NAI)1024376
Feb 16, 2023Tupelo, MSVeterinaryNo Action Indicated (NAI)1018573
Apr 29, 2022Joplin, MOVeterinaryVoluntary Action Indicated (VAI)3003658370
Sep 1, 2021Tupelo, MSVeterinaryOfficial Action Indicated (OAI)1018573
Oct 27, 2020Tupelo, MSVeterinaryOfficial Action Indicated (OAI)1018573
Nov 14, 2019Tupelo, MSVeterinaryNo Action Indicated (NAI)1018573
Sep 30, 2019Halifax, VAVeterinaryNo Action Indicated (NAI)1000158707
Sep 5, 2019Red Bay, ALVeterinaryNo Action Indicated (NAI)1024376
Dec 13, 2018Tupelo, MSVeterinaryOfficial Action Indicated (OAI)1018573
May 16, 2018Dublin, GAVeterinaryNo Action Indicated (NAI)3003273225
Apr 8, 2015Joplin, MOVeterinaryNo Action Indicated (NAI)3003658370
Nov 1, 2012Red Bay, ALVeterinaryNo Action Indicated (NAI)1024376
Aug 25, 2011Tupelo, MSVeterinaryNo Action Indicated (NAI)1018573
Apr 18, 2011Halifax, VAVeterinaryNo Action Indicated (NAI)1000158707
Aug 16, 2010Tupelo, MSVeterinaryNo Action Indicated (NAI)1018573

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 1018573Tupelo, MS8Jun 4, 2026
FEI 1024376Red Bay, AL5May 22, 2026
FEI 3003273225Dublin, GA2May 6, 2026
FEI 3003658370Joplin, MO3Feb 6, 2025
FEI 1000158707Halifax, VA3Sep 30, 2019

FDA data resources

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