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•Croda Iberica SA•August 5, 2019

FDA 483 - Croda Iberica SA - August 05, 2019

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Record Details

An FDA inspection of Croda Iberica SA, an API manufacturer in Fogars de la Selva, Barcelona, Spain, revealed significant deficiencies in their quality systems. Observations included improper storage of stability samples, multiple failures in quality unit responsibilities, and inadequate employee training practices. These issues collectively indicate a lack of adherence to current Good Manufacturing Practices.

Company
Croda Iberica SA
Inspection Date
August 5, 2019
Product Type
Drugs
Office
International Compliance Team
Person
  • Charles L. Zhou (Investigator)
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ID · 2b9113e9-d85a-45bd-9e48-b5389a65402f

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