FDA 483 - Philips North America LLC - March 25, 2020
FDA 483 for Philips North America LLC on March 25, 2020. Product: device. Access full analysis and detailed observations.
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FDA 483 for Philips North America LLC on March 25, 2020. Product: device. Access full analysis and detailed observations.
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Company
Philips North America LLCInspection Date
March 25, 2020
Product Type
device
ID: 667c62b3-1632-4393-8a7d-ed16cdeabb0b
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