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483
•Goodwin Biotechnology, Inc.•April 10, 2019

Goodwin Biotechnology, Inc. – FDA 483, Apr 10, 2019

Record Details

Goodwin Biotechnology, Inc., a drug contract manufacturing and laboratory in Plantation, FL, was inspected by the FDA. The inspection revealed significant deficiencies in laboratory controls, including issues with method validation, bioburden testing, and sterility testing. Additionally, the firm failed to thoroughly review unexplained discrepancies and exhibited inadequate quality control unit procedures, impacting various aspects from SOP revisions to visual inspection and data integrity.

Company
Goodwin Biotechnology, Inc.
Inspection date
April 10, 2019
Product type
drugs
Office
Office of Medical Device and Radiological Health Division II
People
  • Susan T. Hadman (Microbiologist)
  • Jose F. Velez
View Company Profile

ID · ada67b91-cb64-457a-b980-959f36e4368e

Other documents for Goodwin Biotechnology, Inc.
  • 483 - 2025-05-16May 16, 2025

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