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483
•AgileMD, Inc.

FDA 483 - AgileMD, Inc.

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Record Details

This FDA Form 483 was issued to AgileMD, Inc. following an inspection. The report indicates observations made by investigators regarding potential deviations from regulatory requirements. Without specific details, the exact nature and severity of the findings cannot be determined.

Company
AgileMD, Inc.
Product Type
Device
Office
Office of Medical Device and Radiological Health Operations
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ID · b8bdb92f-a255-45b4-ae14-ee86f245e510

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