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483
•Radiometer Basel AG•October 20, 2016

Radiometer Basel AG – FDA 483, Oct 20, 2016

Record Details

Radiometer Basel AG, a medical device manufacturer in Basel, Switzerland, was cited for two significant observations during an FDA inspection. The firm failed to adequately verify design output against design input requirements for its TCM5 monitor and lacked established procedures for controlling nonconforming products. These issues highlight deficiencies in the company's quality system.

Company
Radiometer Basel AG
Inspection date
October 20, 2016
Product type
device
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
Person
  • Stephen D. Eich (investigator)
View Company Profile

ID · 37407e05-4f56-4273-9ea7-1a6371f2254a

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