Gambro Renal Products, Inc.February 16, 2010

FDA 483 - Gambro Renal Products, Inc. - February 16, 2010

Record Details

This FDA Form 483 inspection report for Gambro Renal Products, Inc. indicates that no inspectional observations were cited during the inspection. The report therefore does not detail any specific deficiencies or violations.

Company: Gambro Renal Products, Inc.
Inspection Date: February 16, 2010
Product Type: Device
Office: Division of Advertising & Promotion
Person: Herbert P. Lerner, M.D., Director (Acting)

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ID · 82dacf6e-8c1b-47e0-8af2-533b035fdad9