# Vitrex Medical A/S – FDA Inspection, Jun 1, 2017

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

> FDA inspection 1030486 of Vitrex Medical A/S, June 01, 2017. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1252014 - 2024-09-12

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/natasha-n-mccants/dda403fd-cb19-4cee-93f8-2d4c1c7a8d31)

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