# FDA Inspection 1159339 - NIHON KOHDEN ORANGEMED, INC - December 01, 2021

Source: https://www.keypedia.com/records/fda_inspections/nihon-kohden-orangemed-inc/15ee7ba3-e81f-4058-b84a-6b4c504641a2
Source feed: FDA_Inspections

> FDA Inspection 1159339 for NIHON KOHDEN ORANGEMED, INC on December 01, 2021. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1159339
- Company Name: NIHON KOHDEN ORANGEMED, INC
- Inspection Date: 2021-12-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1159339 - 2021-12-01](https://www.keypedia.com/records/fda_inspections/nihon-kohden-orangemed-inc/c5cc3041-58ed-48f2-8040-227f38644968)

Company: https://www.keypedia.com/companies/nihon-kohden-orangemed-inc/a1c13f0f-ad3a-4dcf-b3fc-8e5228bbd7b0

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