# FDA 483 - Cefla s.c - July 09, 2018

Source: https://www.keypedia.com/records/483/cefla-sc/59cc3e9f-736c-4e3b-a7ce-afc533a5b183

> FDA 483 for Cefla s.c on July 09, 2018. Product: devices. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Cefla s.c
- Inspection Date: 2018-07-09
- Product Type: devices
- Office Name: Center for Devices and Radiological Health
- Summary: The provided content solely comprises information pertaining to FOIA request 2018-6794, released on May 30, 2019, and contact details for FDA/CDRH/OCE/DID. It does not contain the actual substance of an FDA 483 document, making it impossible to extract specifics such as company name, inspection dates, main violations, regulatory framework, or required actions for a summary.

## Related Documents

- [483 - 2018-07-20](https://www.keypedia.com/records/483/cefla-sc/c416adcc-1747-4053-b8ab-b3eec7f1a0e2)

## Related Officers

- [Director](https://www.keypedia.com/people/paolo-bussolari/353cd7e9-66b7-45ac-af14-958af4d1194e)
- [investigator](https://www.keypedia.com/people/jennifer-s-ness/532f8a81-e393-4e83-b5f2-a72362e966de)

Company: https://www.keypedia.com/companies/cefla-sc/4ea6979f-a3a2-48a8-b16c-fe254a5663b0

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