# FDA 483 - MANDELAY KFT - October 17, 2019

Source: https://www.globalkeysolutions.net/records/483/mandelay-kft/19941150-3a85-4604-86c9-10141ab2c4a8

> FDA 483 for MANDELAY KFT on October 17, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: MANDELAY KFT
- Inspection Date: 2019-10-17
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)

## Related Documents

- [WARNING_LETTER - 2019-10-17](https://www.globalkeysolutions.net/records/warning_letter/mandelay-kft/22c2bd07-9dea-444f-8e93-edc1a38fe9b5)

## Related Officers

- [investigator](https://www.globalkeysolutions.net/people/karen-m-rodriguez/fcef1f49-583d-45ab-80e2-4c34793fd722)

Company: https://www.globalkeysolutions.net/companies/mandelay-kft/7f43d01a-bfdb-449d-b4f9-51a87cca1158

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