FDA Inspection 1190753 — Mobius Bionics LLC

Mobius Bionics LLC — FEI 3012481940

The FDA completed an inspection of Mobius Bionics LLC on November 16, 2022 in Manchester, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 16, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Manchester, NH (United States)

Citations

IDCFRDescription
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency