# FDA Inspection 1058697 - Nuvectra Corporation - June 11, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/nuvectra-corporation/2c5e83f9-4e09-4853-bfaf-3fee7e22b4c9
Source feed: FDA_Inspections

> FDA Inspection 1058697 for Nuvectra Corporation on June 11, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1058697
- Company Name: Nuvectra Corporation
- Inspection Date: 2018-06-11
- 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 1058697 - 2018-06-11](https://www.globalkeysolutions.net/records/fda_inspections/nuvectra-corporation/a49186e6-3ef4-4ed7-bf21-26ccb75bf168)
- [FDA Inspection 1016857 - 2017-04-12](https://www.globalkeysolutions.net/records/fda_inspections/nuvectra-corporation/b286e940-7587-4f94-921b-b66362dd9b53)

Company: https://www.globalkeysolutions.net/companies/nuvectra-corporation/f5ad8ad0-616f-4a4a-b554-18d61dd66cb0

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