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483
•Noras MRI Products GmbH•May 17, 2018

Noras MRI Products GmbH – FDA 483, May 17, 2018

Record Details

An FDA inspection of Noras MRT Products GmbH in Hochberg, Germany, revealed four significant quality system deficiencies. The firm failed to adequately review and revalidate processes after changes, maintain device master records, conduct proper risk analysis, and ensure device history records align with master records. These issues indicate a lack of robust quality control in medical device manufacturing.

Company
Noras MRI Products GmbH
Inspection date
May 17, 2018
Product type
device
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
Person
  • Andrew J. Garufi
View Company Profile

ID · 9acc2076-4a71-42ea-ba29-8458f4f4187d

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