# Mueller-Omicron GmbH & Co. KG – FDA Inspection, Nov 15, 2012

Source: https://www.keypedia.com/records/fda_inspections/mueller-omicron-gmbh-co-kg/d3f214e0-58ed-4037-afde-26341c3097ef
Source feed: FDA_Inspections

> FDA inspection 809889 of Mueller-Omicron GmbH & Co. KG, November 15, 2012. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 809889
- Company Name: Mueller-Omicron GmbH & Co. KG
- Inspection Date: 2012-11-15
- 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: 7

Company: https://www.keypedia.com/companies/mueller-omicron-gmbh-co-kg/b9babde2-6840-4dd2-af85-0b9ea626818f

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