# JVC KENWOOD Corporation – FDA Inspection, Oct 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 of JVC KENWOOD Corporation, October 29, 2009. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 945768 - 2015-07-30

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