FDA 483 - CardioFocus, Inc. - August 11, 2022
FDA 483 for CardioFocus, Inc. on August 11, 2022. Product: device. Access full analysis and detailed observations.
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FDA 483 for CardioFocus, Inc. on August 11, 2022. Product: device. Access full analysis and detailed observations.
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Company
CardioFocus, Inc.Inspection Date
August 11, 2022
Product Type
device
ID: 96584ac2-718c-459a-a25d-930f62f39310
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