JABIL SWITZERLAND MANUFACTURING GMBH

FDA Regulatory Profile

JABIL SWITZERLAND MANUFACTURING GMBH has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Mar 12, 2026 · 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
Inspections5Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 12, 2026Le Locle, SwitzerlandDevicesNo Action Indicated (NAI)3015831087
Jun 26, 2025Hagendorf, SwitzerlandDevicesNo Action Indicated (NAI)3015876273
May 14, 2025Grenchen, SwitzerlandDevicesNo Action Indicated (NAI)3015869492
Apr 3, 2025Raron, SwitzerlandDevicesNo Action Indicated (NAI)3015869121
May 5, 2023Le Locle, SwitzerlandDevicesNo Action Indicated (NAI)3015831087

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 3015831087Le Locle, Switzerland2Mar 12, 2026
FEI 3015876273Hagendorf, Switzerland1Jun 26, 2025
FEI 3015869492Grenchen, Switzerland1May 14, 2025
FEI 3015869121Raron, Switzerland1Apr 3, 2025

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