FDA Inspection
JVC KENWOOD CorporationJVC KENWOOD Corporation – FDA Inspection, Oct 29, 2009
Record Details
This FDA Inspection record concerns JVC KENWOOD Corporation, with an inspection on October 29, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- JVC KENWOOD Corporation
- Inspection Date
- October 29, 2009
- Product Type
- Devices
View Company Profile
ID · 5b693ae7-4292-4e3e-8cbd-2d4335011f6d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 634812
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.198(a)(1)Uniform and timely processing
- 21 CFR 820.250(a)Statistical techniques - Lack of or inadequate procedures
- 21 CFR 820.200(d)(5)Service performed
- 21 CFR 820.30(j)Design history file
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Other FDA inspections of JVC KENWOOD Corporation
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 30, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for JVC KENWOOD Corporation
- FDA Inspection 945768 - 2015-07-30
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