FDA Inspection 1263229 — Calyxo, Inc.

Calyxo, Inc. — FEI 3014683069

The FDA completed an inspection of Calyxo, Inc. on Feb 20, 2025 in Pleasanton, CA. 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
Feb 20, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Pleasanton, CA (United States)