# FDA 483 - Maquet SAS - February 01, 2018

Source: https://www.globalkeysolutions.net/records/483/maquet-sas/79dd44c1-6754-4d84-aacd-12a711699108

> FDA 483 for Maquet SAS on February 01, 2018. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Maquet SAS
- Inspection Date: 2018-02-01
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)

## Related Documents

- [483 - Unknown Date](https://www.globalkeysolutions.net/records/483/maquet-sas/76859f56-fbd8-4dd1-b73b-f4c04166bf31)
- [483 - 2025-01-16](https://www.globalkeysolutions.net/records/483/maquet-sas/6a029879-bc9b-4eb0-b0c0-9a76009a6314)

## Related Officers

- [Medical Device Senior Operations Officer at FDA](https://www.globalkeysolutions.net/people/thomas-a-peter/48a36892-cc03-42bb-8960-978d18f2147a)

Company: https://www.globalkeysolutions.net/companies/maquet-sas/7e2d533e-d7fc-4715-b60c-928657757140

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