# Ziehm Imaging Gmbh – FDA Inspection, Feb 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/ziehm-imaging-gmbh/f01297db-5910-4998-9813-bebb17da8ef2
Source feed: FDA_Inspections

> FDA inspection 1006562 of Ziehm Imaging Gmbh, February 17, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 820 and 1010. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1006562
- Company Name: Ziehm Imaging Gmbh
- Inspection Date: 2017-02-17
- 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

## Related Documents

- FDA Inspection 892023 - 2014-08-07
- [FDA Inspection 791614 - 2012-06-28](https://www.keypedia.com/records/fda_inspections/ziehm-imaging-gmbh/fe400f2f-6caf-4aec-b6d8-eb5e1c6cf26b)

## Related Officers

- Andrew Saunders

Company: https://www.keypedia.com/companies/ziehm-imaging-gmbh/03deeaf1-0b2a-4d7b-ab56-038fc6443fee

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