Home / Inspections / 842224

FDA Inspection 842224 — Dornier Medtech America, Inc.

Dornier Medtech America, Inc. — FEI 1037955

The FDA completed an inspection of Dornier Medtech America, Inc. on May 31, 2013 in Kennesaw, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 31, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Kennesaw, GA (United States)

Facility

Other inspections at this facility

  • 1028402 (NAI Thu Aug 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 653108 (VAI Fri Mar 05 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources