# FDA Inspection 634812 - JVC KENWOOD Corporation - October 29, 2009

Source: https://www.keypedia.com/records/fda_inspections/jvc-kenwood-corporation/5b693ae7-4292-4e3e-8cbd-2d4335011f6d
Source feed: FDA_Inspections

> FDA Inspection 634812 for JVC KENWOOD Corporation on October 29, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 634812
- Company Name: JVC KENWOOD Corporation
- Inspection Date: 2009-10-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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