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483
•Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)•February 9, 2018

Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) – FDA 483, Feb 9, 2018

Record Details

An FDA inspection of Vetter Pharma Fertigung Gmbg & Co. KG in Ravensburg, Germany, identified a significant issue regarding the firm's risk assessment processes. Specifically, the assessment supporting media fills lacked comprehensive details and evaluations. This indicates a moderate severity finding related to quality control and manufacturing practices.

Company
Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
Inspection date
February 9, 2018
Product type
drugs
Office
Office of Inspections and Investigations
People
  • Thuy T. Nguyen ( Investigator, Consumer Safety Officer)
  • Michael R. Klapal (Investigator)
View Company Profile

ID · d2c2a04a-70fd-47d0-9898-d4c6ae6f5b44

Other documents for Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
  • 483 - 2024-03-19March 19, 2024
  • 483 - 2022-08-26August 26, 2022
  • 483 - 2017-11-02November 2, 2017
  • EIR - 2016-07-16July 16, 2016
  • 483

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