# FDA Inspection 1032232 - Nuvectra Corporation - October 31, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/nuvectra-corporation/66e03c46-fff5-4c3f-8ed4-91ccb24dda68
Source feed: FDA_Inspections

> FDA Inspection 1032232 for Nuvectra Corporation on October 31, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1032232
- Company Name: Nuvectra Corporation
- Inspection Date: 2017-10-31
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/nuvectra-corporation/78c66107-cf42-4a98-8607-d1cf5368f551

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