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

Record Details

This FDA Inspection record concerns Dornier Medtech America, Inc., with an inspection on March 5, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Dornier Medtech America, Inc.
Inspection Date: March 5, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4a11e76e-75ae-4e14-b486-f30b6c8e4043

Violation Codes3

21 CFR 803.50(a)(1)21 CFR 820.100(b)21 CFR 820.198(b)

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