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    FDA Form 483 for Delpharm Dijon Human Drugs Inspection Ending May 2024

    FDA Form 483 for Delpharm Dijon Human Drugs Inspection Ending May 2024

    $69.00 USD
    $69.00 USD
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    Original Request: Please share the Form 483 for Delpharm Dijon Inspection ended on May 31, 2024 for the site Quetigny, France and fei id 3014120699. The inspection was related to Human Drugs.
    Tags: Pharma, 483, 2024
    • 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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