# FDA Inspection 1088972 - Nihon Kohden America LLC - April 30, 2019

Source: https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/715540c2-32fb-44bd-b143-9643c4e99bb2
Source feed: FDA_Inspections

> FDA Inspection 1088972 for Nihon Kohden America LLC on April 30, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088972
- Company Name: Nihon Kohden America LLC
- Inspection Date: 2019-04-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/nihon-kohden-america-llc/6d634199-3448-4668-ae42-2ca3ea095b6a

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