# FDA Inspection 1258826 - Plexus Corp. - January 22, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/plexus-corp/ac1ed3d1-1641-4dac-86e4-24673b94ce40
Source feed: FDA_Inspections

> FDA Inspection 1258826 for Plexus Corp. on January 22, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1258826
- Company Name: Plexus Corp.
- Inspection Date: 2025-01-22
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1258826 - 2025-01-22](https://www.globalkeysolutions.net/records/fda_inspections/plexus-corp/38782fe5-6df2-460a-a316-aed73f3c5c30)
- [FDA Inspection 1258826 - 2025-01-22](https://www.globalkeysolutions.net/records/fda_inspections/plexus-corp/f63ff5c3-a752-4d02-8533-d64dc777bf60)
- [FDA Inspection 1258826 - 2025-01-22](https://www.globalkeysolutions.net/records/fda_inspections/plexus-corp/f8d9c37d-2e07-4d81-b2cb-44ba2994ff18)
- [FDA Inspection 663288 - 2010-05-11](https://www.globalkeysolutions.net/records/fda_inspections/plexus-corp/b663ac73-265b-4401-9d1d-769989be9c51)

Company: https://www.globalkeysolutions.net/companies/plexus-corp/8364d9e7-527e-41c0-9826-b7f58e400226

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