# FDA Inspection 762022 - Nihon Kohden Tomioka Corporation - December 09, 2011

Source: https://www.keypedia.com/records/fda_inspections/nihon-kohden-tomioka-corporation/4f22c994-d1c9-49c7-b413-96fbb551d08a
Source feed: FDA_Inspections

> FDA Inspection 762022 for Nihon Kohden Tomioka Corporation on December 09, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 762022
- Company Name: Nihon Kohden Tomioka Corporation
- Inspection Date: 2011-12-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 971813 - 2016-03-25](https://www.keypedia.com/records/fda_inspections/nihon-kohden-tomioka-corporation/543bca1f-f6ba-4f6b-b3a3-81d143d017a7)

Company: https://www.keypedia.com/companies/nihon-kohden-tomioka-corporation/853cabd2-c931-4c8f-8c7a-95535094b8ee

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