# FDA Inspection 817926 - ERBE Elektromedizin GmbH - January 31, 2013

Source: https://www.keypedia.com/records/fda_inspections/erbe-elektromedizin-gmbh/0280a8a3-ee80-40b3-9a67-18d9fd03fa7d
Source feed: FDA_Inspections

> FDA Inspection 817926 for ERBE Elektromedizin GmbH on January 31, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 817926
- Company Name: ERBE Elektromedizin GmbH
- Inspection Date: 2013-01-31
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 817926 - 2013-01-31](https://www.keypedia.com/records/fda_inspections/erbe-elektromedizin-gmbh/ca330c87-7069-4751-ba54-fcf413147b20)

Company: https://www.keypedia.com/companies/erbe-elektromedizin-gmbh/4e42fea1-c912-46c1-a08f-23c47cc2b7f5

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