# FDA Inspection 1053875 - Ushio America, Inc. - May 31, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/ushio-america-inc/e7db790d-3ced-49e7-9cec-d39b5cc86b99
Source feed: FDA_Inspections

> FDA Inspection 1053875 for Ushio America, Inc. on May 31, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1053875
- Company Name: Ushio America, Inc.
- Inspection Date: 2018-05-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1053875 - 2018-05-31](https://www.globalkeysolutions.net/records/fda_inspections/ushio-america-inc/d143eb8c-43c3-4bab-a03c-540b3e742836)
- [FDA Inspection 1053875 - 2018-05-31](https://www.globalkeysolutions.net/records/fda_inspections/ushio-america-inc/e3813808-1914-4d4d-a128-afdc361f7cae)

Company: https://www.globalkeysolutions.net/companies/ushio-america-inc/b8a9fd54-c8ed-49b5-8624-f926c4f53310

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