# FDA Inspection 953978 - V. Guldmann A/S - December 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/v-guldmann-as/944db2d8-7b23-45a0-8fe6-25649dc5d4e6
Source feed: FDA_Inspections

> FDA Inspection 953978 for V. Guldmann A/S on December 17, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 953978
- Company Name: V. Guldmann A/S
- Inspection Date: 2015-12-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/v-guldmann-as/ab0288ee-b9e8-4443-9d0d-a9c723e08f1c

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