FDA 483_RESPONSE - Mayo Clinic Pharmacy - August 10, 2018

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Record Details

This 483 RESPONSE record concerns Mayo Clinic Pharmacy, with an inspection on August 10, 2018, issued by the Office of Health Technology 2 (Cardiovascular Devices), covering devices.

Company: Mayo Clinic Pharmacy
Inspection Date: August 10, 2018
Product Type: Devices
Office: Office of Health Technology 2 (Cardiovascular Devices)
People: Art O. Czabaniuk (Program Division Director)
Kevin R. Dillon

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ID · 14772710-9a0c-413d-9de5-89d7cdcf934c

Violation Codes1

21 U.S.C. 331

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