# FDA Inspection 1100385 - USHIO GERMANY GmbH - August 23, 2019

Source: https://www.keypedia.com/records/fda_inspections/ushio-germany-gmbh/b9da4ca1-c231-4d81-a2bb-6eee0d6712b1
Source feed: FDA_Inspections

> FDA Inspection 1100385 for USHIO GERMANY GmbH on August 23, 2019. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1100385
- Company Name: USHIO GERMANY GmbH
- Inspection Date: 2019-08-23
- Classification: Official Action Indicated (OAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100385 - 2019-08-23](https://www.keypedia.com/records/fda_inspections/ushio-germany-gmbh/53c6ade7-b7a8-48f4-b50c-f981f73b546b)

Company: https://www.keypedia.com/companies/ushio-germany-gmbh/9331ee4d-d19a-4851-9de3-948e3f24a47a

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