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483
•Fenwal International, Inc.•April 25, 2023

Fenwal International, Inc. – FDA 483, Apr 25, 2023

Record Details

Fenwal International, Inc., a medical device manufacturer in Bajos De Haina, Dominican Republic, was cited with seven observations during an FDA inspection from April 17-25, 2023. The inspection revealed significant deficiencies in quality system procedures, including inadequate control of non-conforming products, insufficient corrective and preventive actions, unsuitable building design for cleanroom operations, and poor equipment maintenance and process control. These issues indicate a systemic lack of adherence to quality system regulations for medical device manufacturing.

Company
Fenwal International, Inc.
Inspection date
April 25, 2023
Product type
device
Office
International Compliance Team
People
  • Scott T. Ballard
  • Creighton T. Tuzon
View Company Profile

ID · 5f4657e4-6ed1-4f69-9447-bd7e983c624a

Other documents for Fenwal International, Inc.
  • WARNING_LETTER - 2019-09-26September 26, 2019

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