# VE Valley Electronics GmbH – FDA Inspection, Oct 18, 2012

Source: https://www.keypedia.com/records/fda_inspections/ve-valley-electronics-gmbh/1f022514-90dd-4292-9457-0e82d8e756fc
Source feed: FDA_Inspections

> FDA inspection 806462 of VE Valley Electronics GmbH, October 18, 2012. Classification: Official Action Indicated (OAI). 8 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 806462
- Company Name: VE Valley Electronics GmbH
- Inspection Date: 2012-10-18
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

Company: https://www.keypedia.com/companies/ve-valley-electronics-gmbh/9c79a37f-71dc-4d47-992d-d7c3c0d381c5

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