Primo Brands

FDA Regulatory Profile

Primo Brands has 0 FDA recalls, 21 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 24, 2026 · NAI

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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
Inspections21Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 24, 2026Ft Lauderdale, FLFood/CosmeticsNo Action Indicated (NAI)1035882
May 26, 2026Chatsworth, CAFood/CosmeticsNo Action Indicated (NAI)3004291464
Apr 28, 2026Amarillo, TXFood/CosmeticsNo Action Indicated (NAI)1620793
Apr 14, 2026Nashville, TNFood/CosmeticsNo Action Indicated (NAI)3004341743
Apr 7, 2026Scott, LAFood/CosmeticsNo Action Indicated (NAI)3004297604
Nov 10, 2025Cortlandt Manor, NYFood/CosmeticsNo Action Indicated (NAI)3023816784
Sep 22, 2025Wichita Falls, TXFood/CosmeticsNo Action Indicated (NAI)3004276700
Jun 27, 2025Brawley, CAFood/CosmeticsNo Action Indicated (NAI)2013306
Jun 3, 2025Midland, TXFood/CosmeticsNo Action Indicated (NAI)1621393
May 22, 2025Cabazon, CAFood/CosmeticsNo Action Indicated (NAI)3004425056
Aug 6, 2018Midland, TXFood/CosmeticsNo Action Indicated (NAI)1621393
Jun 5, 2018Victorville, CAFood/CosmeticsNo Action Indicated (NAI)3008776363
Nov 16, 2017Brawley, CAFood/CosmeticsNo Action Indicated (NAI)2013306
Sep 13, 2017Midland, TXFood/CosmeticsNo Action Indicated (NAI)1621393
Jun 27, 2017Scott, LAFood/CosmeticsVoluntary Action Indicated (VAI)3004297604
Mar 29, 2016Nashville, TNFood/CosmeticsNo Action Indicated (NAI)3004341743
Jan 17, 2013Nashville, TNFood/CosmeticsNo Action Indicated (NAI)3004341743
Aug 9, 2012Cabazon, CAFood/CosmeticsNo Action Indicated (NAI)3004425056
Jul 29, 2011Ft Lauderdale, FLFood/CosmeticsNo Action Indicated (NAI)1035882
Nov 4, 2010Brawley, CAFood/CosmeticsNo Action Indicated (NAI)2013306

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 1035882Ft Lauderdale, FL3Sep 24, 2026
FEI 3004291464Chatsworth, CA1May 26, 2026
FEI 1620793Amarillo, TX1Apr 28, 2026
FEI 3004341743Nashville, TN3Apr 14, 2026
FEI 3004297604Scott, LA2Apr 7, 2026
FEI 3023816784Cortlandt Manor, NY1Nov 10, 2025
FEI 3004276700Wichita Falls, TX1Sep 22, 2025
FEI 2013306Brawley, CA3Jun 27, 2025
FEI 1621393Midland, TX3Jun 3, 2025
FEI 3004425056Cabazon, CA2May 22, 2025
FEI 3008776363Victorville, CA1Jun 5, 2018

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