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483
•Laboratoires Urgo•December 11, 2017

Laboratoires Urgo – FDA 483, Dec 11, 2017

Record Details

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.

Company
Laboratoires Urgo
Inspection date
December 11, 2017
Product type
devices
Office
Center for Devices and Radiological Health
People
  • Marie-Catherine Sarciaux (Quality Director)
  • Mary A. Millner
View Company Profile

ID · a4aeb48b-5a6e-4e8a-9cfd-5ff309770d0c

Other documents for Laboratoires Urgo
  • 483 - 2017-12-14December 14, 2017

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