# FDA Inspection 965257 - Medtronic Mexico EG - February 12, 2016

Source: https://www.keypedia.com/records/fda_inspections/medtronic-mexico-eg/6206d3fc-22bf-40be-a06d-e52c7f4c5d0c
Source feed: FDA_Inspections

> FDA Inspection 965257 for Medtronic Mexico EG on February 12, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 965257
- Company Name: Medtronic Mexico EG
- Inspection Date: 2016-02-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 965257 - 2016-02-12](https://www.keypedia.com/records/fda_inspections/medtronic-mexico-eg/234fee47-83af-47be-895b-0d3001b85fe2)
- [FDA Inspection 852089 - 2013-08-22](https://www.keypedia.com/records/fda_inspections/medtronic-mexico-eg/317e304a-c059-4fa2-9cb3-6ff302f7bdeb)
- [FDA Inspection 852089 - 2013-08-22](https://www.keypedia.com/records/fda_inspections/medtronic-mexico-eg/761b1d64-ab60-4ced-8846-04f89352e6bf)

Company: https://www.keypedia.com/companies/medtronic-mexico-eg/6d77ebb6-d70f-4f06-be16-79b51be10a30

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