# FDA Inspection 904773 - Physiomed Elektromedizin AG - November 07, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/physiomed-elektromedizin-ag/fdeee083-e704-4662-8c2f-8cea7ff31a15/
Source feed: FDA_Inspections

> FDA Inspection 904773 for Physiomed Elektromedizin AG on November 07, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 904773
- Company Name: Physiomed Elektromedizin AG
- Inspection Date: 2014-11-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 904773 - 2014-11-07](https://www.globalkeysolutions.net/api/records/fda_inspections/physiomed-elektromedizin-ag/91675831-798f-42d5-9d2f-eec1602a494f/)

Company: https://www.globalkeysolutions.net/companies/physiomed-elektromedizin-ag/3ebca620-5c98-4c96-bd35-0fb351121912

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