# Dornier Medtech America, Inc. – FDA Inspection, Mar 5, 2010

Source: https://www.keypedia.com/records/fda_inspections/dornier-medtech-america-inc/b7dc3882-df93-4fe0-819d-b74438a1438a
Source feed: FDA_Inspections

> FDA inspection 653108 of Dornier Medtech America, Inc., March 05, 2010. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 653108
- Company Name: Dornier Medtech America, Inc.
- Inspection Date: 2010-03-05
- 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: 3

## Related Documents

- FDA Inspection 1028402 - 2017-08-24
- FDA Inspection 842224 - 2013-05-31

Company: https://www.keypedia.com/companies/dornier-medtech-america-inc/15c4c247-5610-407c-b659-4d42e5407be0

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