FDA Inspection 1233777 — Endotronix, Inc.

Endotronix, Inc. — FEI 3024985933

The FDA completed an inspection of Endotronix, Inc. on Feb 27, 2024 in Naperville, IL. 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 27, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Naperville, IL (United States)