483
STX-Med SPRLSTX-Med SPRL – FDA 483
Record Details
This FDA Form 483 report pertains to an inspection conducted at STX-Med SPRL. Without specific observation details, the report indicates potential deviations from regulatory requirements identified during the inspection. The full scope and severity of the findings are not detailed here.
- Company
- STX-Med SPRL
- Product type
- device
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ID · 9abe43ba-2b67-4149-afe2-ae14c7f9eb8d
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