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FDA Form 483 – Knox Medical Diagnostics, Inc. (FEI 3016721526), Aug 2024
FDA Form 483 – Knox Medical Diagnostics, Inc. (FEI 3016721526), Aug 2024
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Original Request: To Whom it May Concern: As permitted by the Freedom of Information Act (FOIA), I am hereby requesting the following document: Form FDA 483: Knox Medical Diagnostics, Inc. San Francisco, California United States End Dates of inspection: 21 Aug 2024 Project Area: Compliance: Devices FEI: 3016721526 Classification: VAI I confirm that Clarivate Analytics will be charged accordingly by FOI for this request, however please contact me if the charges exceed $ 200.
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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