FDA 483_RESPONSE - Alexion Pharmaceuticals, Inc. - August 06, 2012

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Record Details

This 483 RESPONSE record concerns Alexion Pharmaceuticals, Inc., with an inspection on August 6, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Alexion Pharmaceuticals, Inc.
Inspection Date: August 6, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health
People: Jolanna A. (Medical Content Writer)
Ann Farrell
Cornelius Dunn
Tonia F (Investigator)
Yashwant Amin (Dr.)

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ID · cd134dee-ba34-4656-9408-2174ed4228a3

Violation Codes1

21 CFR 210

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