# FDA 483 - Biotronik SE & Co. KG - June 23, 2022

Source: https://www.globalkeysolutions.net/records/483/biotronik-se-co-kg/c417df4d-301e-4ab4-85c1-e8f5b4435908

> FDA 483 for Biotronik SE & Co. KG on June 23, 2022. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Biotronik SE & Co. KG
- Inspection Date: 2022-06-23
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)

## Related Officers

- [Dedicated Device Cadre](https://www.globalkeysolutions.net/people/dedicated-device-cadre/693932db-dd86-453f-9b51-a63444b07281)
- [Cso](https://www.globalkeysolutions.net/people/daniel-j-lahar/d4e329c0-b6a5-42ca-acde-b79413b245ea)

Company: https://www.globalkeysolutions.net/companies/biotronik-se-co-kg/8a12b042-671e-4374-a012-562a49b35594

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