FDA Inspection 1242541 — Endotronix, Inc.

Endotronix, Inc. — FEI 3024985933

The FDA completed an inspection of Endotronix, Inc. on Jun 11, 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
Jun 11, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Naperville, IL (United States)

Additional Details

Sponsor, Contract Research Organization