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483
•Magellan Diagnostics, Inc.•August 26, 2025

Magellan Diagnostics, Inc. – FDA 483, Aug 26, 2025

Record Details

Magellan Diagnostics, Inc. in North Billerica, MA, was inspected regarding its blood lead testing systems. The inspection revealed significant deficiencies across multiple quality system areas, including inadequate corrective and preventive actions, design verification, process validation, incoming product acceptance, and risk analysis. Furthermore, the firm failed to timely report numerous medical device malfunctions and a field correction to the FDA, indicating a systemic breakdown in quality management and regulatory compliance that could impact patient safety.

Company
Magellan Diagnostics, Inc.
Inspection date
August 26, 2025
Product type
device
Office
New England District Office
Person
  • Sunita Pandey
View Company Profile

ID · 91db7bc5-1928-4ba5-bd82-f3ad3a452377

Other documents for Magellan Diagnostics, Inc.
  • 483 - 2021-06-22June 22, 2021
  • 483 - 2019-10-21October 21, 2019
  • WARNING_LETTER - 2017-06-29June 29, 2017
  • 483 - 2017-06-29June 29, 2017

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