# FDA Inspection 859242 - Rominger Medizintechnik GmbH - December 11, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/rominger-medizintechnik-gmbh/4528543b-450f-4ddc-8c80-14cfb25420bb
Source feed: FDA_Inspections

> FDA Inspection 859242 for Rominger Medizintechnik GmbH on December 11, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 859242
- Company Name: Rominger Medizintechnik GmbH
- Inspection Date: 2013-12-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1064786 - 2018-09-05](https://www.globalkeysolutions.net/records/fda_inspections/rominger-medizintechnik-gmbh/6ec1fcf0-54c7-4e4d-a0dd-2a0b48559a22)
- [FDA Inspection 1064786 - 2018-09-05](https://www.globalkeysolutions.net/records/fda_inspections/rominger-medizintechnik-gmbh/b0fb3b21-d8f0-46ce-a237-9aad09308ff0)

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

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