# FDA Inspection 653108 - Dornier Medtech America, Inc. - March 05, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/dornier-medtech-america-inc/4a11e76e-75ae-4e14-b486-f30b6c8e4043
Source feed: FDA_Inspections

> FDA Inspection 653108 for Dornier Medtech America, Inc. on March 05, 2010. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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