# Biotronik, AG – FDA Inspection, Mar 17, 2016

Source: https://www.keypedia.com/records/fda_inspections/biotronik-ag/c7cf23ee-302f-48be-b11f-fae3d3fcf525
Source feed: FDA_Inspections

> FDA inspection 967279 of Biotronik, AG, March 17, 2016. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 967279
- Company Name: Biotronik, AG
- Inspection Date: 2016-03-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

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- [FDA Inspection 1089612 - 2018-03-09](https://www.keypedia.com/records/fda_inspections/biotronik-ag/f1eb24d7-12b8-46aa-a268-fa810095cee7)
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Company: https://www.keypedia.com/companies/biotronik-ag/b17190ac-395d-4442-9297-12bd60fe1464

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