FDA Inspection 1006694 — Senseonics, Inc.

Senseonics, Inc. — FEI 3009862700

The FDA completed an inspection of Senseonics, Inc. on April 4, 2017 in Germantown, MD. 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
April 4, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Germantown, MD (United States)