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    FDA Form 483 – Meridian Medical Technologies, LLC Inspection (Saint Louis, 12/21/2019, FEI 1950222)

    FDA Form 483 – Meridian Medical Technologies, LLC Inspection (Saint Louis, 12/21/2019, FEI 1950222)

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    Request Contents: FDA Form 483 for Meridian Medical Technologies, LLC, a subsidiary of Kindeva Drug Delivery, L.P. Inspection ended on Dec 21, 2019, for the Saint Louis, United States site (FEI 1950222). Inspection related to Medical Devices and Rad Health.
    • Status: Pending Fast-Track Request
    • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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