FDA Inspection 1169088 — Orthalign, Inc

Orthalign, Inc — FEI 3007521480

The FDA completed an inspection of Orthalign, Inc on April 28, 2022 in Aliso Viejo, CA. 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
April 28, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Aliso Viejo, CA (United States)