FDA Inspection 1310648 — Jabil Switzerland Manufacturing GmbH

Jabil Switzerland Manufacturing GmbH — FEI 3015831087

The FDA completed an inspection of Jabil Switzerland Manufacturing GmbH on March 12, 2026 in Le Locle. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 12, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Le Locle (Switzerland)