# FDA 483 - Medtronic Neurological - January 24, 2007

Source: https://www.keypedia.com/records/483/medtronic-neurological/93a7fd86-79e3-4d3c-b33b-03e5f327127e

> FDA 483 for Medtronic Neurological on January 24, 2007. Product: Devices. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Medtronic Neurological
- Inspection Date: 2007-01-24
- Product Type: Devices
- Office Name: Minneapolis District Office
- Summary: I am sorry, but I cannot create a summary of the FDA 483 document as the provided content only contains page numbers and does not include the actual text of the inspection report. Please provide the full text of the report for analysis so I can extract the company name, inspection dates, main violations/issues, regulatory framework, and required actions.

## Related Officers

- [Consumer Safety Officer](https://www.keypedia.com/people/jocelyn-muggli/0651c073-56c4-4646-a7e0-6bd925fe2961)
- [investigator](https://www.keypedia.com/people/timothy-phillips/f10e8c3a-6cbe-4ad0-ac1b-abcfdb6074bf)

Company: https://www.keypedia.com/companies/medtronic-neurological/258ed721-b3e6-4441-86eb-3de39fdb6f54

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d