# FDA 483 - U-Needle B.V. - April 12, 2019

Source: https://www.globalkeysolutions.net/records/483/u-needle-bv/b6223f5f-155a-487a-92da-598874c31e4a

> FDA 483 for U-Needle B.V. on April 12, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: U-Needle B.V.
- Inspection Date: 2019-04-12
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
- Summary: 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.

## Related Officers

- [Rumi Young](https://www.globalkeysolutions.net/people/rumi-young/7ce96abb-ccae-40ee-8bcd-d5f44bee499b)

Company: https://www.globalkeysolutions.net/companies/u-needle-bv/4e2ac1da-5097-48c1-b409-5a301cb48686

Office: https://www.globalkeysolutions.net/offices/division-of-clinical-evidence-and-analysis-1-clinical-policy-and-quality/5f95da17-30bb-423f-b892-5ea041823fbd