# Auric Hoersysteme Gmbh & Co.kg – FDA Inspection, Nov 12, 2009

Source: https://www.keypedia.com/records/fda_inspections/auric-hoersysteme-gmbh-cokg/a484ad77-0f16-401a-b668-471e1df16432
Source feed: FDA_Inspections

> FDA inspection 629680 of Auric Hoersysteme Gmbh & Co.kg, November 12, 2009. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 629680
- Company Name: Auric Hoersysteme Gmbh & Co.kg
- Inspection Date: 2009-11-12
- 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

Company: https://www.keypedia.com/companies/auric-hoersysteme-gmbh-cokg/835208a1-5438-469c-b9b7-5bc1e89c8cd9

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