FDA 483_RESPONSE - CareFirst Specialty Pharmacy LLC - November 30, 2022

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Record Details

This 483 RESPONSE record concerns CareFirst Specialty Pharmacy LLC, with an inspection on November 30, 2022, issued by the Office of Health Technology 5 (Neurological and Physical Medicine Devices), covering devices.

Company: CareFirst Specialty Pharmacy LLC
Inspection Date: November 30, 2022
Product Type: Devices
Office: Office of Health Technology 5 (Neurological and Physical Medicine Devices)
People: Lisa M. Harlan (Program Division Director)
Satish V. Poondi

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ID · 06542004-d8b3-47c0-93e8-d774dd9b82c0

Violation Codes1

FD&C Act 501(a)(2)(A)

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