FDA Inspection 1180599 — Premia Spine Inc.

Premia Spine Inc. — FEI 3012452928

The FDA completed an inspection of Premia Spine Inc. on Sep 23, 2022 in Norwalk, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 23, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Norwalk, CT (United States)

Additional Details

Sponsor, Contract Research Organization