FDA Inspection 1192361 — Ortho2

Ortho2 — FEI 3009149931

The FDA completed an inspection of Ortho2 on December 1, 2022 in Ames, IA. 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 1, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Ames, IA (United States)