# FDA Inspection 818837 - Biotronik, AG - January 24, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/biotronik-ag/83a27c10-33d8-4817-9870-e9a58bc919cc
Source feed: FDA_Inspections

> FDA Inspection 818837 for Biotronik, AG on January 24, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 818837
- Company Name: Biotronik, AG
- Inspection Date: 2013-01-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1087258 - 2019-01-24](https://www.globalkeysolutions.net/records/fda_inspections/biotronik-ag/baf0e612-65e4-4e7b-b338-2b37de30d1ef)
- [FDA Inspection 967279 - 2016-03-17](https://www.globalkeysolutions.net/records/fda_inspections/biotronik-ag/c7cf23ee-302f-48be-b11f-fae3d3fcf525)
- [FDA Inspection 967279 - 2016-03-17](https://www.globalkeysolutions.net/records/fda_inspections/biotronik-ag/471dbc6f-7832-452b-8b0e-16f2bb8ad52c)
- [FDA Inspection 947090 - 2015-09-24](https://www.globalkeysolutions.net/records/fda_inspections/biotronik-ag/5ef1c31d-c743-465d-8705-395113e438e6)
- [FDA Inspection 947090 - 2015-09-24](https://www.globalkeysolutions.net/records/fda_inspections/biotronik-ag/72cdaf23-9e05-42e3-8d8f-213cb43a7e3b)

Company: https://www.globalkeysolutions.net/companies/biotronik-ag/b17190ac-395d-4442-9297-12bd60fe1464

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
