Company
United StatesDornier Medtech America, Inc., Kennesaw, GA – FDA Inspections
Inspection records and compliance data for Dornier Medtech America, Inc. in Kennesaw, Georgia. 3 FDA inspections on record, last inspected August 24, 2017.
Company Profile
This profile covers Dornier Medtech America, Inc. based in Kennesaw, Georgia, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 1
- NAI
- 2
- Form 483s
- 0
- Warning letters
- 0
First inspected March 5, 2010. Last inspected August 24, 2017.
Most cited issue areas
- Procedures1 inspection
- Report of Death or Serious Injury1 inspection
- Review and evaluation for investigation1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| August 24, 2017 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1028402 |
| May 31, 2013 | NAI | Medical Devices & Rad Health · Compliance: Devices | 842224 |
| March 5, 2010 | VAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 653108 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Dornier Medtech America, Inc.
FEI Number
1037955
Address
1155 Roberts Blvd NW, Kennesaw, Georgia 30144, United States
Country
United States
ID: 15c4c247-5610-407c-b659-4d42e5407be0