FDA 483 - DuoProSS Meditech Corporation - August 12, 2022
FDA 483 for DuoProSS Meditech Corporation on August 12, 2022. Product: device. Access full analysis and detailed observations.
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FDA 483 for DuoProSS Meditech Corporation on August 12, 2022. Product: device. Access full analysis and detailed observations.
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Inspection Date
August 12, 2022
Product Type
device
ID: 49c4ae37-ab47-4d79-ba44-faba0f3dc35f
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