# FDA Inspection 1067019 - Aurident Inc - September 27, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/aurident-inc/941dab2f-17cc-4389-865b-9bf80a8f0861
Source feed: FDA_Inspections

> FDA Inspection 1067019 for Aurident Inc on September 27, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1067019
- Company Name: Aurident Inc
- Inspection Date: 2018-09-27
- 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 1067019 - 2018-09-27](https://www.globalkeysolutions.net/records/fda_inspections/aurident-inc/ef8aaa1e-94be-4115-b2a7-e15b627b3e50)
- [FDA Inspection 816456 - 2013-01-29](https://www.globalkeysolutions.net/records/fda_inspections/aurident-inc/653bbd96-c1e0-4de9-aa35-ea368fdcf535)
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Company: https://www.globalkeysolutions.net/companies/aurident-inc/498bd7dc-e80f-4ded-a3cf-4aef0103af22

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