# Rominger Medizintechnik GmbH – FDA Inspection, Sep 5, 2018

Source: https://www.keypedia.com/records/fda_inspections/rominger-medizintechnik-gmbh/b0fb3b21-d8f0-46ce-a237-9aad09308ff0
Source feed: FDA_Inspections

> FDA inspection 1064786 of Rominger Medizintechnik GmbH, September 05, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064786
- Company Name: Rominger Medizintechnik GmbH
- Inspection Date: 2018-09-05
- 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: 3

## Related Documents

- FDA Inspection 859242 - 2013-12-11

## Related Officers

- [Investigator](https://www.keypedia.com/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

Company: https://www.keypedia.com/companies/rominger-medizintechnik-gmbh/cf43d615-587a-4703-bea1-64da0b4e8d51

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