# FDA Inspection 773877 - Beurer North America, LLC - March 26, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/beurer-north-america-llc/8255bae1-df14-4a78-b032-4b37f8cf4b6c
Source feed: FDA_Inspections

> FDA Inspection 773877 for Beurer North America, LLC on March 26, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 773877
- Company Name: Beurer North America, LLC
- Inspection Date: 2012-03-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 773877 - 2012-03-26](https://www.globalkeysolutions.net/records/fda_inspections/beurer-north-america-llc/6a7b0750-3b8d-4f47-8276-402f5410613a)
- [FDA Inspection 773877 - 2012-03-26](https://www.globalkeysolutions.net/records/fda_inspections/beurer-north-america-llc/dd7e4ed2-06d9-4446-ac5f-aebf376e010a)

Company: https://www.globalkeysolutions.net/companies/beurer-north-america-llc/de507472-5ee2-40a6-bcdc-267a4685310f

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