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483
•Eckert & Ziegler Radiopharma GmbH•August 19, 2019

Eckert & Ziegler Radiopharma GmbH – FDA 483, Aug 19, 2019

Record Details

Eckert & Ziegler Radiopharma GmbH, a manufacturer of radiopharmaceutical APIs in Berlin, Germany, was cited for significant deficiencies in environmental control, monitoring, and data integrity during an FDA inspection. Observations included inadequate smoke studies, lack of particle monitoring, unvalidated disinfectant efficacy, and issues with software audit trails and investigation practices. The findings indicate a need for improved aseptic processing controls and quality system oversight.

Company
Eckert & Ziegler Radiopharma GmbH
Inspection date
August 19, 2019
Product type
drugs
Office
Office of Biological Products Operations - Division I
Person
  • Jose A. Cruz Gonzalez
View Company Profile

ID · 8349eeda-44e1-48d5-9b05-9fdab10fd2d8

Other documents for Eckert & Ziegler Radiopharma GmbH
  • 483 - 2022-07-07July 7, 2022

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