Bonaterra Products Inc.

FDA Regulatory Profile

Bonaterra Products Inc. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jun 23, 2026 · VAI

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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
Inspections8Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 23, 2026South El Monte, CAFood/CosmeticsVoluntary Action Indicated (VAI)3005295282
Jul 28, 2022South El Monte, CAFood/CosmeticsVoluntary Action Indicated (VAI)3005295282
Nov 13, 2018South El Monte, CAFood/CosmeticsNo Action Indicated (NAI)3005295282
Nov 29, 2017South El Monte, CAFood/CosmeticsNo Action Indicated (NAI)3005295282
Nov 14, 2014South El Monte, CAFood/CosmeticsNo Action Indicated (NAI)3005295282
Feb 8, 2012South El Monte, CAFood/CosmeticsNo Action Indicated (NAI)3005295282
Aug 19, 2011South El Monte, CAFood/CosmeticsOfficial Action Indicated (OAI)3005295282
Jan 14, 2011South El Monte, CAFood/CosmeticsOfficial Action Indicated (OAI)3005295282

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 3005295282South El Monte, CA8Jun 23, 2026

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