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483
•Alexion Pharmaceuticals, Inc.•March 7, 2025

Alexion Pharmaceuticals, Inc. – FDA 483, Mar 7, 2025

Record Details

An FDA inspection of Alexion Pharmaceuticals, Inc. in Boston, MA, revealed a significant issue regarding the firm's compliance with its approved REMS Implementation System for the drug Voydeya. The company failed to adhere to its audit plan and schedule for certified pharmacies and did not maintain adequate records to ensure restricted distribution of the medication. This indicates a moderate severity issue related to drug distribution controls and oversight.

Company
Alexion Pharmaceuticals, Inc.
Inspection date
March 7, 2025
Product type
drugs
Office
New England District Office
Person
  • Meredith L. Miller
View Company Profile

ID · a419172e-26c2-47cb-9836-f572daa92416

Other documents for Alexion Pharmaceuticals, Inc.
  • 483 - 2024-11-07November 7, 2024
  • WARNING_LETTER - 2012-08-06August 6, 2012

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