# FDA 483 - DFS Diamon GmbH - September 20, 2019

Source: https://www.globalkeysolutions.net/records/483/dfs-diamon-gmbh/064e1ec7-df48-4725-a249-c15785783ba7

> FDA 483 for DFS Diamon GmbH on September 20, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: DFS Diamon GmbH
- Inspection Date: 2019-09-20
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)

## Related Officers

- [Dedicated Device Cadre](https://www.globalkeysolutions.net/people/dedicated-device-cadre/693932db-dd86-453f-9b51-a63444b07281)
- [investigator](https://www.globalkeysolutions.net/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.globalkeysolutions.net/companies/dfs-diamon-gmbh/02748a3f-0960-4b2b-b9d8-3d45dc19bb6a

Office: https://www.globalkeysolutions.net/offices/division-of-clinical-evidence-and-analysis-1-clinical-policy-and-quality/5f95da17-30bb-423f-b892-5ea041823fbd