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Technology / Good manufacturing practice / Form FDA 483 / Center for Devices and Radiological Health / Medical device / Design controls / Quality management system / QSIT / Title 21 of the Code of Federal Regulations / Food and Drug Administration / Medicine / Health
Technology
Good manufacturing practice
Form FDA 483
Center for Devices and Radiological Health
Medical device
Design controls
Quality management system
QSIT
Title 21 of the Code of Federal Regulations
Food and Drug Administration
Medicine
Health

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