# FDA 483 - Laboratoires Urgo - December 11, 2017

Source: https://www.keypedia.com/records/483/laboratoires-urgo/a4aeb48b-5a6e-4e8a-9cfd-5ff309770d0c

> FDA 483 for Laboratoires Urgo on December 11, 2017. Product: devices. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Laboratoires Urgo
- Inspection Date: 2017-12-11
- Product Type: devices
- Office Name: Center for Devices and Radiological Health
- Summary: The provided text exclusively contains administrative information related to Freedom of Information Act (FOIA) request 2018-1113, including its release date of October 28, 2019, and contact details for FDA/CDRH/OCE/DID. This content does not include any substantive details typically found in an FDA 483 document. Specifically, there is no mention of a company name, the dates when an inspection was conducted, any identified main violations or issues, the specific regulatory framework under which observations were made, or any required actions to address deficiencies. Consequently, it is not possible to generate a concise summary of an FDA 483 document, which would typically detail inspection findings and regulatory requirements, based on the provided input. The text solely provides a record of a FOIA processing event rather than the content of an FDA 483 itself.

## Related Documents

- [483 - 2017-12-14](https://www.keypedia.com/records/483/laboratoires-urgo/bf4fd0bf-e331-4611-a8d2-13231a7df763)

## Related Officers

- [Mary A. Millner](https://www.keypedia.com/people/mary-a-millner/bd8911cf-849d-41d2-ae12-dd4bad66e798)
- [Quality Director](https://www.keypedia.com/people/marie-catherine-sarciaux/cb727fa5-8bd3-424d-9e1a-6c9d4a6010b8)

Company: https://www.keypedia.com/companies/laboratoires-urgo/778edcaf-341c-48fe-939c-c5ddb29b12b8

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