FDA Inspection 1269031 — Calvary Spine, LLC

Calvary Spine, LLC — FEI 3007279845

The FDA completed an inspection of Calvary Spine, LLC on May 2, 2025 in Towson, MD. 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
May 2, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Towson, MD (United States)

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