# DETAX GmbH & Co. KG – FDA Inspection, Apr 6, 2018

Source: https://www.keypedia.com/records/fda_inspections/detax-gmbh-co-kg/ed8b25bb-7fb7-4b21-999d-1eef2a8f5d0f
Source feed: FDA_Inspections

> FDA inspection 1047145 of DETAX GmbH & Co. KG, April 06, 2018. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1047145
- Company Name: DETAX GmbH & Co. KG
- Inspection Date: 2018-04-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/kelvin-cheung/ded61aee-4b4b-4049-a67c-19d971475be7)

Company: https://www.keypedia.com/companies/detax-gmbh-co-kg/0b21b841-e097-4684-9829-78be38a82594

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