FDA Inspection 1271578 — Mobius Mobility LLC

Mobius Mobility LLC — FEI 3014522447

The FDA completed an inspection of Mobius Mobility LLC on May 14, 2025 in Manchester, NH. 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
May 14, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Manchester, NH (United States)

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