FDA Inspection 1256410 — Soulaire Corporation

Soulaire Corporation — FEI 3031814196

The FDA completed an inspection of Soulaire Corporation on December 5, 2024 in Santa Monica, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
December 5, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Monica, CA (United States)