# Dornier Medtech America, Inc., Kennesaw, GA – FDA Inspections

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

> Inspection records and compliance data for Dornier Medtech America, Inc. in Kennesaw, Georgia. 3 FDA inspections on record, last inspected August 24, 2017.

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## Details

- Name: Dornier Medtech America, Inc.
- FEI Number: 1037955
- Address Line 1: 1155 Roberts Blvd NW
- City: Kennesaw
- State: Georgia
- Zip Code: 30144
- Country Name: United States
- Address: 1155 Roberts Blvd NW, Kennesaw, Georgia 30144, United States
- Country: United States

## Related Documents

- FDA Inspection 1028402 - Dornier Medtech America, Inc. - 2017-08-24 — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2017
- FDA Inspection 1028402 - Dornier Medtech America, Inc. - 2017-08-24 — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2017
- FDA Inspection 1028402 - Dornier Medtech America, Inc. - 2017-08-24 — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2017
- FDA Inspection 842224 - Dornier Medtech America, Inc. - 2013-05-31 — classification: No Action Indicated (NAI), source: FDA, date: May 31, 2013
- FDA Inspection 842224 - Dornier Medtech America, Inc. - 2013-05-31 — classification: No Action Indicated (NAI), source: FDA, date: May 31, 2013
- FDA Inspection 653108 - Dornier Medtech America, Inc. - 2010-03-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 5, 2010
- [FDA Inspection 653108 - Dornier Medtech America, Inc. - 2010-03-05](https://www.keypedia.com/records/fda_inspections/dornier-medtech-america-inc/b7dc3882-df93-4fe0-819d-b74438a1438a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 5, 2010

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