FDA Inspection 1089930 — Axonics, Inc.

Axonics, Inc. — FEI 3002968685

The FDA completed an inspection of Axonics, Inc. on May 2, 2019 in Irvine, CA. 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
May 2, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)