FDA Inspection 1085016 — Avitus Orthopaedics, Inc.

Avitus Orthopaedics, Inc. — FEI 3011504993

The FDA completed an inspection of Avitus Orthopaedics, Inc. on Feb 28, 2019 in Shelton, CT. 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
Feb 28, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Shelton, CT (United States)