# FDA Inspection 1296772 - MEDTRONIC GRAND RAPIDS - December 15, 2025

Source: https://www.keypedia.com/records/fda_inspections/medtronic-grand-rapids/d2b55e97-bd71-4587-bc85-54f658df073f
Source feed: FDA_Inspections

> FDA Inspection 1296772 for MEDTRONIC GRAND RAPIDS on December 15, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1296772
- Company Name: MEDTRONIC GRAND RAPIDS
- Inspection Date: 2025-12-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Detroit District Office

## Related Documents

- [FDA Inspection 1296772 - 2025-12-15](https://www.keypedia.com/records/fda_inspections/medtronic-grand-rapids/0f58e005-86fc-4735-94bb-14767aaac6cb)
- [FDA Inspection 1296772 - 2025-12-15](https://www.keypedia.com/records/fda_inspections/medtronic-grand-rapids/00593b94-35a3-4838-80ec-75ef3804d9fc)
- [FDA Inspection 1296772 - 2025-12-15](https://www.keypedia.com/records/fda_inspections/medtronic-grand-rapids/40503c12-b77f-456d-a5a6-1d59c24cc2f1)

Company: https://www.keypedia.com/companies/medtronic-grand-rapids/1863d548-4a7c-4559-816b-991360c608f4

Office: https://www.keypedia.com/offices/detroit-district-office/b09a1815-a000-40c0-bb44-5432ce87ed03