Jasper Wyman & Son

FDA Regulatory Profile

Jasper Wyman & Son has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 19, 2026 · NAI

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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
Inspections6Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 19, 2026Cherryfield, MEFood/CosmeticsNo Action Indicated (NAI)1211427
Sep 15, 2025Jonesboro, MEFood/CosmeticsNo Action Indicated (NAI)3004382397
Sep 20, 2023Cherryfield, MEFood/CosmeticsVoluntary Action Indicated (VAI)1211427
Jan 18, 2018Jonesboro, MEFood/CosmeticsNo Action Indicated (NAI)3004382397
Nov 30, 2017Ellsworth, MEFood/CosmeticsNo Action Indicated (NAI)1211375
Dec 3, 2012Jonesboro, MEFood/CosmeticsNo Action Indicated (NAI)3004382397

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 1211427Cherryfield, ME2Aug 19, 2026
FEI 3004382397Jonesboro, ME3Sep 15, 2025
FEI 1211375Ellsworth, ME1Nov 30, 2017

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