# FDA Inspection 945768 - JVC KENWOOD Corporation - July 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/jvc-kenwood-corporation/5b8aed00-b637-40d2-94d6-96ff0db43c01
Source feed: FDA_Inspections

> FDA Inspection 945768 for JVC KENWOOD Corporation on July 30, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 945768
- Company Name: JVC KENWOOD Corporation
- Inspection Date: 2015-07-30
- 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 945768 - 2015-07-30](https://www.keypedia.com/records/fda_inspections/jvc-kenwood-corporation/1fd9f384-1778-4524-9a41-b45204df1ad2)
- [FDA Inspection 634812 - 2009-10-29](https://www.keypedia.com/records/fda_inspections/jvc-kenwood-corporation/5b693ae7-4292-4e3e-8cbd-2d4335011f6d)

Company: https://www.keypedia.com/companies/jvc-kenwood-corporation/506778ba-896e-49c8-9fa2-ecb01cbb4846

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