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483
•Boehringer Ingelheim RCV GmbH & Co KG•December 5, 2023

Boehringer Ingelheim RCV GmbH & Co KG – FDA 483, Dec 5, 2023

Record Details

An FDA inspection of Boehringer Ingelheim RCV GmbH & Co KG in Vienna, Austria, a manufacturer of drug substances, identified two significant observations. The firm's Standard Operating Procedures for critical shipping steps were found to be inadequate, lacking details on loading duration and container activation. Additionally, equipment preventive maintenance was deemed insufficient, resulting in frequent malfunctions and seal leaks on final container bottle head tubing for several drug substance batches.

Company
Boehringer Ingelheim RCV GmbH & Co KG
Inspection date
December 5, 2023
Product type
biologics
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
People
  • Tate Armin
  • Prajakta Vasantkar
View Company Profile

ID · 060b49d8-c11a-4a49-b649-a1e4f4140363

Other documents for Boehringer Ingelheim RCV GmbH & Co KG
  • 483 - 2023-12-05December 5, 2023
  • 483 - 2023-11-16November 16, 2023
  • 483 - 2018-11-19November 19, 2018

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