# FDA Inspection 1034520 - Sequent Medical, Inc. - November 16, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/sequent-medical-inc/df3fe2f3-9af1-4ada-974c-9f81f93fdef6
Source feed: FDA_Inspections

> FDA Inspection 1034520 for Sequent Medical, Inc. on November 16, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1034520
- Company Name: Sequent Medical, Inc.
- Inspection Date: 2017-11-16
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1044416 - 2018-02-16](https://www.globalkeysolutions.net/records/fda_inspections/sequent-medical-inc/9503cfa3-bbde-4c70-ae06-87c920be579c)
- [FDA Inspection 1034520 - 2017-11-16](https://www.globalkeysolutions.net/records/fda_inspections/sequent-medical-inc/7ac52259-601b-43cf-8f75-84c4b741ec9f)
- [FDA Inspection 834024 - 2013-05-30](https://www.globalkeysolutions.net/records/fda_inspections/sequent-medical-inc/f47f8d8a-a73b-488b-a66a-03db6e8dd242)
- [FDA Inspection 834024 - 2013-05-30](https://www.globalkeysolutions.net/records/fda_inspections/sequent-medical-inc/cf1f5071-8d7c-4367-87a7-68c73bf65000)

Company: https://www.globalkeysolutions.net/companies/sequent-medical-inc/f49dd887-1645-4704-8307-dc282315ab5c

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
