# FDA Inspection 931993 - Dufner Instrumente GmbH - June 25, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/dufner-instrumente-gmbh/df938a7f-5fc6-4b3f-96bf-458f00ef1890
Source feed: FDA_Inspections

> FDA Inspection 931993 for Dufner Instrumente GmbH on June 25, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 931993
- Company Name: Dufner Instrumente GmbH
- Inspection Date: 2015-06-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1232698 - 2024-03-13](https://www.globalkeysolutions.net/records/fda_inspections/dufner-instrumente-gmbh/5cdad011-037f-4ee1-82f9-61b3f0d9c65a)
- [FDA Inspection 931993 - 2015-06-25](https://www.globalkeysolutions.net/records/fda_inspections/dufner-instrumente-gmbh/8ccb6da3-2a74-4f15-95b5-a8bd4d5a1da1)
- [FDA Inspection 669440 - 2010-06-10](https://www.globalkeysolutions.net/records/fda_inspections/dufner-instrumente-gmbh/6fa0c93d-f4fa-471d-8b12-6860f9899c0b)

Company: https://www.globalkeysolutions.net/companies/dufner-instrumente-gmbh/8166b55d-1cb6-4e0e-9420-61abb8c14aaa

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