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FDA Inspection
•Synapse Biomedical Inc•October 7, 2020

Synapse Biomedical Inc – FDA Inspection, Oct 7, 2020

Record Details

This FDA Inspection record concerns Synapse Biomedical Inc, with an inspection on October 7, 2020, issued by the Center for Devices and Radiological Health, covering devices.

Company
Synapse Biomedical Inc
Inspection Date
October 7, 2020
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 9ab8d3d4-e900-4bb9-85b0-2e5bf1e06081

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
1130955
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Synapse Biomedical Inc

4
DateClassificationOfficeProject area
January 18, 2023NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 5, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
November 5, 2012VAICenter for Devices and Radiological HealthBioresearch Monitoring
February 11, 2010VAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Synapse Biomedical Inc
  • FDA Inspection 1195865 - 2023-01-18
  • FDA Inspection 906473 - 2014-12-05
  • FDA Inspection 807042 - 2012-11-05
  • FDA Inspection 644078 - 2010-02-11

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