Ashland Specialty Ingredients, G.P.

FDA Regulatory Profile

Ashland Specialty Ingredients, G.P. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 22, 2025 · 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
Inspections5Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 22, 2025Fiskeville, RIDevicesVoluntary Action Indicated (VAI)3010785603
Sep 10, 2025Hopewell, VAFood/CosmeticsNo Action Indicated (NAI)1110870
Aug 7, 2025Bridgewater, NJDevicesVoluntary Action Indicated (VAI)1000122243
Feb 17, 2023Bridgewater, NJDevicesVoluntary Action Indicated (VAI)1000122243
Nov 21, 2017Bridgewater, NJDevicesNo Action Indicated (NAI)1000122243

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 3010785603Fiskeville, RI1Dec 22, 2025
FEI 1110870Hopewell, VA1Sep 10, 2025
FEI 1000122243Bridgewater, NJ3Aug 7, 2025

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