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    FDA Form 483 – Medical Device Inspections (4 Firms Listed – May 2024)

    FDA Form 483 – Medical Device Inspections (4 Firms Listed – May 2024)

    $69.00 USD
    $69.00 USD
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    Original Request: Please provide the FDA-483 documents pertaining to Medical Device Inspection Inspection, for the following 4 firms: Calmare Therapeutics, Inc., 2 Trap Falls Rd Ste 507, Shelton, CT, United States, (FEI: 3006435903), inspection ending 5/22/2024; Criticare Technologies, Inc., 333 Strawberry Field Rd Ste 11, Warwick, RI, United States, (FEI: 3012238587), inspection ending 5/10/2024; Cumberland Biotherapeutics LLC, 1565 Jackson Point Rd,ETC
    • 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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