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FDA Inspection
•Robert Bosch Healthcare Systems, Inc.•May 22, 2013

Robert Bosch Healthcare Systems, Inc. – FDA Inspection, May 22, 2013

Record Details

This FDA Inspection record concerns Robert Bosch Healthcare Systems, Inc., with an inspection on May 22, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Robert Bosch Healthcare Systems, Inc.
Inspection Date
May 22, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · dc284351-469c-45fc-8b6e-35b5a106a22b

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
833686
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Robert Bosch Healthcare Systems, Inc.

1
DateClassificationOfficeProject area
July 21, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Robert Bosch Healthcare Systems, Inc.
  • FDA Inspection 936848 - 2015-07-21

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