FDA Inspection 1192938 — Atlas Spine, Inc.

Atlas Spine, Inc. — FEI 3003855635

The FDA completed an inspection of Atlas Spine, Inc. on December 6, 2022 in Jupiter, FL. 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
December 6, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jupiter, FL (United States)