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    FDA Form 483s for Keranetics Inc., Angiodynamics Inc., and Others – Medical Device Inspections

    FDA Form 483s for Keranetics Inc., Angiodynamics Inc., and Others – Medical Device Inspections

    $69.00 USD
    $69.00 USD
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    Original Request: Please provide the following inspection-related document(s) in electronic PDF format of ProductType: Devices: The 483(s) (in electronic format) for the inspection of Keranetics Inc. (FEI 3015980493), located in Winston Salem, North Carolina, United States, inspection ending 2025-02-06, with project area(s): Compliance: Devices, Postmarket Assurance: Devices. The 483(s) (in electronic format) for the inspection of Angiodynamics, Inc. (FEI 1319211), located in Queensbury, New York, United States, inspection ending 2025-01-10, with project area(s): Compliance: Devices, Postmarket Assurance: Devices. ETC
    Tags: MedTech, 483, 2025
    • 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. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.

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