# FDA Inspection 976895 - Medtronic Perfusion Systems - June 17, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/medtronic-perfusion-systems/f65aacdc-c341-4fbf-88e1-238a0b868a34/
Source feed: FDA_Inspections

> FDA Inspection 976895 for Medtronic Perfusion Systems on June 17, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 976895
- Company Name: Medtronic Perfusion Systems
- Inspection Date: 2016-06-17
- 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 976895 - 2016-06-17](https://www.globalkeysolutions.net/api/records/fda_inspections/medtronic-perfusion-systems/8e778d17-2262-41bf-9a46-85494c578e7c/)
- [FDA Inspection 808091 - 2012-11-19](https://www.globalkeysolutions.net/api/records/fda_inspections/medtronic-perfusion-systems/b64b38a8-f370-429d-a22b-712469c68a5e/)
- [FDA Inspection 808091 - 2012-11-19](https://www.globalkeysolutions.net/api/records/fda_inspections/medtronic-perfusion-systems/6765af24-55a5-4b3e-8b84-ffcfdabc1d1a/)
- [FDA Inspection 659025 - 2010-04-28](https://www.globalkeysolutions.net/api/records/fda_inspections/medtronic-perfusion-systems/2e11eafe-e024-4bc1-8e00-6e0b514eede1/)

Company: https://www.globalkeysolutions.net/companies/medtronic-perfusion-systems/7670713a-7115-4348-9dc7-9ce5fda8e6fd

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