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483
•Schoelly Fiberoptic GmbH•September 27, 2023

Schoelly Fiberoptic GmbH – FDA 483, Sep 27, 2023

Record Details

This document is an FDA Form 483 issued to Schoelly Fiberoptic GmbH. No specific inspectional observations or findings are detailed in the provided text, which appears to be administrative information related to a FOIA request.

Company
Schoelly Fiberoptic GmbH
Inspection date
September 27, 2023
Product type
device
Office
Office of Medical Device and Radiological Health Operations
Person
  • Sandra Baumann
View Company Profile

ID · fcf20cb4-2f89-4dcd-80d1-b28d113eb08f

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