# FDA Inspection 1252486 - Nihon Kohden America LLC - October 04, 2024

Source: https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/b7c73937-488a-475c-91d9-1adda8869bbb
Source feed: FDA_Inspections

> FDA Inspection 1252486 for Nihon Kohden America LLC on October 04, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1252486
- Company Name: Nihon Kohden America LLC
- Inspection Date: 2024-10-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1252486 - 2024-10-04](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/345c2181-1220-48e5-9d10-8f7bc9615807)
- [FDA Inspection 1252486 - 2024-10-04](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/1f281d46-cbc6-4216-aec3-143313a2337f)
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- [FDA Inspection 1088972 - 2019-04-30](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/b95e490b-83a8-4ea8-915f-659ea44130e9)

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