FDA Inspection 1192938 — Atlas Spine, Inc.

Atlas Spine, Inc. — FEI 3003855635

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.