# Medart A /S – FDA Inspection, Sep 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/medart-a-s/b7351a72-ea04-4a85-9113-7e59bcdcf351
Source feed: FDA_Inspections

> FDA inspection 849997 of Medart A /S, September 13, 2013. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803, 820, 1002 and 1040. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 849997
- Company Name: Medart A /S
- Inspection Date: 2013-09-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1053704 - 2018-05-31](https://www.keypedia.com/records/fda_inspections/medart-a-s/f8ee9721-a5ca-43ec-819a-805b393d4521)
- FDA Inspection 944716 - 2015-09-24
- [FDA Inspection 789470 - 2012-06-01](https://www.keypedia.com/records/fda_inspections/medart-a-s/c4d812c2-c81b-42d1-913c-75482b98c5bf)

Company: https://www.keypedia.com/companies/medart-a-s/ab57d5ff-3427-4a6e-8de0-632843e359f7

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