FDA Inspection 1195865 — Synapse Biomedical Inc

Synapse Biomedical Inc — FEI 3005868392

The FDA completed an inspection of Synapse Biomedical Inc on January 18, 2023 in Oberlin, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 18, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Oberlin, OH (United States)