# FDA Inspection 1040786 - Nihon Kohden America LLC - October 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/ec0effbe-7583-4a4f-96d8-246783364bbd
Source feed: FDA_Inspections

> FDA Inspection 1040786 for Nihon Kohden America LLC on October 26, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1040786
- Company Name: Nihon Kohden America LLC
- Inspection Date: 2017-10-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: 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/b7c73937-488a-475c-91d9-1adda8869bbb)
- [FDA Inspection 1252486 - 2024-10-04](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/1f281d46-cbc6-4216-aec3-143313a2337f)
- [FDA Inspection 1142130 - 2021-05-03](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/e0e8869c-7832-447d-a465-4e1c9da1c8c4)
- [FDA Inspection 1142130 - 2021-05-03](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/e80a9dda-c86b-43bf-bd24-db5805922bc0)

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