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

Source: https://www.globalkeysolutions.net/records/483_response/mayo-clinic-pharmacy/14772710-9a0c-413d-9de5-89d7cdcf934c

> FDA 483_RESPONSE for Mayo Clinic Pharmacy on August 10, 2018. Product: Devices. Access full analysis and detailed observations.

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## Details

- Record Type: 483_RESPONSE
- Company Name: Mayo Clinic Pharmacy
- Inspection Date: 2018-08-10
- Product Type: Devices
- Office Name: Office of Health Technology 2 (Cardiovascular Devices)

## Related Documents

- [STATE_REFERRAL_LETTER - 2018-08-10](https://www.globalkeysolutions.net/records/state_referral_letter/mayo-clinic-pharmacy/7fe799d0-e6bf-4094-8c44-a8efa1211fbd)
- [483 - 2018-08-15](https://www.globalkeysolutions.net/records/483/mayo-clinic-pharmacy/ae89ec4a-91a3-4725-ae4f-e823f6f342f0)

## Related Officers

- [Program Division Director](https://www.globalkeysolutions.net/people/art-o-czabaniuk/37f1e249-9ee6-4275-9c28-391d93659b85)
- [Kevin R. Dillon](https://www.globalkeysolutions.net/people/kevin-r-dillon/3febc4bb-29d6-4c71-9564-e116fe7e2e84)

Company: https://www.globalkeysolutions.net/companies/mayo-clinic-pharmacy/fb0699ba-f561-46a6-a62c-75da4edf1733

Office: https://www.globalkeysolutions.net/offices/office-of-health-technology-2-cardiovascular-devices/a1c6b7e9-1526-46e5-b040-4400f2e5d821