FDA Inspection 1221034 — MediBeacon, Inc

MediBeacon, Inc — FEI 3027576156

The FDA completed an inspection of MediBeacon, Inc on Oct 13, 2023 in Saint Louis, MO. 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
Oct 13, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Sponsor, Contract Research Organization