# FDA 483 - D-Eye srl - October 08, 2018

Source: https://www.keypedia.com/records/483/d-eye-srl/e864514e-3d7a-42cf-b4f7-71c67b8c7a0c

> FDA 483 for D-Eye srl on October 08, 2018. Product: devices. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: D-Eye srl
- Inspection Date: 2018-10-08
- Product Type: devices
- Office Name: Center for Devices and Radiological Health
- Summary: The provided document content consists solely of information related to an FDA FOIA request (2018-9469) and contact details for FDA/CDRH/OCE/DID. It does not contain any details regarding a specific company, inspection dates, main violations or issues, a regulatory framework, or any required actions from an FDA 483 document. Therefore, a concise summary of an FDA 483 document, including the requested elements, cannot be generated from the given text.

## Related Officers

- [investigator](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)
- [Chief Executive Officer](https://www.keypedia.com/people/alberto-scarpa/e4db724d-ec38-4d6e-b17a-ca20cb1979f2)

Company: https://www.keypedia.com/companies/d-eye-srl/3c55b75b-3a16-40c3-b812-6c9ff4c40dab

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