# FDA Inspection 1030486 - Vitrex Medical A/S - June 01, 2017

Source: https://www.keypedia.com/records/fda_inspections/vitrex-medical-as/f18438e4-cf5f-4e3e-b07d-aa30b2e0daea
Source feed: FDA_Inspections

> FDA Inspection 1030486 for Vitrex Medical A/S on June 01, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030486
- Company Name: Vitrex Medical A/S
- Inspection Date: 2017-06-01
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/vitrex-medical-as/c98a6cc0-cffa-4b3d-8991-e419155b92d8

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