# FDA Inspection 1238904 - Medistri SA - May 09, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/medistri-sa/00871f12-2fd3-453b-8842-dcee4f7ab9d3
Source feed: FDA_Inspections

> FDA Inspection 1238904 for Medistri SA on May 09, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1238904
- Company Name: Medistri SA
- Inspection Date: 2024-05-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1238904 - 2024-05-09](https://www.globalkeysolutions.net/records/fda_inspections/medistri-sa/8fda6c91-cfd8-4eaa-9c68-24799db135f1)
- [FDA Inspection 1087831 - 2019-01-31](https://www.globalkeysolutions.net/records/fda_inspections/medistri-sa/0eb253ca-90db-420a-9d4c-21918be0905e)
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Company: https://www.globalkeysolutions.net/companies/medistri-sa/8cfed4a9-8805-433d-a1c0-14bed6d7f7f1

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