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BlueTriton Brands Hollis

FDA Regulatory Profile

BlueTriton Brands Hollis has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 29, 2022 · 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
Inspections4Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 29, 2022Hollis Center, MEFood/CosmeticsNo Action Indicated (NAI)3003113111
Apr 14, 2017Hollis Center, MEFood/CosmeticsNo Action Indicated (NAI)3003113111
Dec 1, 2009Hollis Center, MEFood/CosmeticsNo Action Indicated (NAI)3003113111
Jul 13, 2009Hollis Center, MEFood/CosmeticsNo Action Indicated (NAI)3003113111

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 3003113111Hollis Center, ME4Sep 29, 2022

FDA data resources

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