# Ushio America, Inc. – FDA Inspection, May 31, 2018

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

> FDA inspection 1053875 of Ushio America, Inc., May 31, 2018. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Officers

- Issuing Officer

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

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