FDA Inspection 1314902 — Moser-Baer AG

Moser-Baer AG — FEI 3007441485

The FDA completed an inspection of Moser-Baer AG on Apr 9, 2026 in Sumiswald. 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 9, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Sumiswald (Switzerland)

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