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Ames Goldsmith Corporation

FDA Regulatory Profile

Ames Goldsmith Corporation has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 22, 2025 · VAI

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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
Inspections9Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 22, 2025Glens Falls, NYDrugsVoluntary Action Indicated (VAI)1317366
Mar 6, 2020Glens Falls, NYDrugsVoluntary Action Indicated (VAI)1317366
Jun 16, 2016Glens Falls, NYDrugsVoluntary Action Indicated (VAI)1317366
Jun 25, 2014Glens Falls, NYDrugsVoluntary Action Indicated (VAI)1317366
Jan 10, 2013Glens Falls, NYDrugsVoluntary Action Indicated (VAI)1317366
Jan 26, 2012Glens Falls, NYDrugsVoluntary Action Indicated (VAI)1317366
Apr 21, 2011Glens Falls, NYDrugsVoluntary Action Indicated (VAI)1317366
Apr 26, 2010Glens Falls, NYDrugsVoluntary Action Indicated (VAI)1317366
Mar 5, 2009Glens Falls, NYDrugsVoluntary Action Indicated (VAI)1317366

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 1317366Glens Falls, NY9May 22, 2025

FDA data resources

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