JW North America, Inc.

FDA Regulatory Profile

JW North America, Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 4, 2025 · 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 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 4, 2025Rockland, MADevicesNo Action Indicated (NAI)1450790
Jun 20, 2019Rockland, MADevicesVoluntary Action Indicated (VAI)1450790
Nov 15, 2018Cartersville, GADevicesVoluntary Action Indicated (VAI)1000110800
Oct 25, 2017Cartersville, GADevicesNo Action Indicated (NAI)1000110800
Sep 22, 2017Rockland, MADevicesNo Action Indicated (NAI)1450790
Sep 21, 2015Rockland, MADevicesVoluntary Action Indicated (VAI)1450790

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 1450790Rockland, MA4Dec 4, 2025
FEI 1000110800Cartersville, GA2Nov 15, 2018

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