# ORGENTEC Diagnostika Gmbh – FDA Inspection, May 2, 2013

Source: https://www.keypedia.com/records/fda_inspections/orgentec-diagnostika-gmbh/d0c075bd-21d6-4503-9cec-d22c4c9c515c
Source feed: FDA_Inspections

> FDA inspection 835430 of ORGENTEC Diagnostika Gmbh, May 02, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 835430
- Company Name: ORGENTEC Diagnostika Gmbh
- Inspection Date: 2013-05-02
- 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: 2

Company: https://www.keypedia.com/companies/orgentec-diagnostika-gmbh/7ea00a00-6ab4-4c91-844c-3c5660d9866a

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