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
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ID · b8bdb92f-a255-45b4-ae14-ee86f245e510