# Medartis AG – FDA Inspection, Aug 27, 2009

Source: https://www.keypedia.com/records/fda_inspections/medartis-ag/a2ff6894-582c-4e95-918d-ab0f15b41dcb
Source feed: FDA_Inspections

> FDA inspection 623342 of Medartis AG, August 27, 2009. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 623342
- Company Name: Medartis AG
- Inspection Date: 2009-08-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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Company: https://www.keypedia.com/companies/medartis-ag/7058fbae-9dc1-4270-8066-73e17b811bd1

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