FDA Inspection 1130955 — Synapse Biomedical Inc

Synapse Biomedical Inc — FEI 3005868392

The FDA completed an inspection of Synapse Biomedical Inc on October 7, 2020 in Oberlin, OH. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
October 7, 2020
Fiscal Year
2021
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Oberlin, OH (United States)