# FDA Inspection 1102180 - Medtronic Neuromodulation - August 06, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/medtronic-neuromodulation/ffaaee90-31c0-4a0a-8024-c623571f25d7/
Source feed: FDA_Inspections

> FDA Inspection 1102180 for Medtronic Neuromodulation on August 06, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1102180
- Company Name: Medtronic Neuromodulation
- Inspection Date: 2019-08-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1206222 - 2023-05-05](https://www.globalkeysolutions.net/api/records/fda_inspections/medtronic-neuromodulation/0d67b0cf-c5ee-4657-8149-1b9c652318b7/)
- [FDA Inspection 1206222 - 2023-05-05](https://www.globalkeysolutions.net/api/records/fda_inspections/medtronic-neuromodulation/ca41952b-debf-4e58-9a3d-a67b671f3055/)
- [FDA Inspection 1187313 - 2022-11-03](https://www.globalkeysolutions.net/api/records/fda_inspections/medtronic-neuromodulation/0826f3ee-c543-4555-ad61-9cede8f200b3/)
- [FDA Inspection 1187313 - 2022-11-03](https://www.globalkeysolutions.net/api/records/fda_inspections/medtronic-neuromodulation/a6f03870-6753-4fb1-ada9-63df4eba6325/)
- [FDA Inspection 1153966 - 2021-09-09](https://www.globalkeysolutions.net/api/records/fda_inspections/medtronic-neuromodulation/67d9522f-cf08-409f-bdb3-699362a190ad/)

Company: https://www.globalkeysolutions.net/companies/medtronic-neuromodulation/2a0b2563-ee1c-4a97-a37a-e714223e0f65

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