483 RESPONSE
Alexion Pharmaceuticals, Inc.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.
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ID · cd134dee-ba34-4656-9408-2174ed4228a3
Violation Codes1
21 CFR 210
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