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FDA Inspection 1028402 — Dornier Medtech America, Inc.

Dornier Medtech America, Inc. — FEI 1037955

The FDA completed an inspection of Dornier Medtech America, Inc. on August 24, 2017 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
August 24, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Kennesaw, GA (United States)

Facility

Other inspections at this facility

  • 842224 (NAI Fri May 31 2013 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