FDA Inspection 1268362 — JABIL SWITZERLAND MANUFACTURING GMBH

JABIL SWITZERLAND MANUFACTURING GMBH — FEI 3015869121

The FDA completed an inspection of JABIL SWITZERLAND MANUFACTURING GMBH on Apr 3, 2025 in Raron. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 3, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Raron (Switzerland)

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