483
U-Needle B.V.FDA 483 - U-Needle B.V. - April 12, 2019
Record Details
This FDA Form 483 report for U-Needle B.V. indicates no inspectional observations were cited. The inspection found no significant issues requiring corrective action, suggesting a compliant operation.
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ID · cbd194a1-6011-46dd-804a-a21d0cf2414b