# Mayo Clinic PET Radiochemistry Facility, Rochester, MN – FDA Inspections

Source: https://www.keypedia.com/companies/mayo-clinic-pet-radiochemistry-facility/6b2304d3-2e0e-4a40-9b2d-5a95a9a873cf

> Inspection records and compliance data for Mayo Clinic PET Radiochemistry Facility in Rochester, Minnesota. 5 FDA inspections on record, 1 Form 483, last inspected September 24, 2025.

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## Details

- Name: Mayo Clinic PET Radiochemistry Facility
- FEI Number: 3009119769
- Business Operations: POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION
- Address Line 1: 200 1st St Sw
- City: Rochester
- State: Minnesota
- Zip Code: 55905
- Country Name: United States
- Address: 200 1st St Sw, Rochester, Minnesota 55905, United States
- Country: United States

## Related Documents

- [483 - Mayo Clinic PET Radiochemistry Facility - 2025-09-24](https://www.keypedia.com/records/483/mayo-clinic-pet-radiochemistry-facility/d79fe46b-fb84-455f-ad32-1c2c96fea706) — source: FDA, date: September 24, 2025
- [FDA Inspection 1283146 - Mayo Clinic PET Radiochemistry Facility - 2025-09-24](https://www.keypedia.com/records/fda_inspections/mayo-clinic-pet-radiochemistry-facility/c91c66f9-8ab5-4221-a1ea-da5c7e4d5377) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 24, 2025
- FDA Inspection 950152 - Mayo Clinic PET Radiochemistry Facility - 2015-12-04 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 4, 2015
- FDA Inspection 937220 - Mayo Clinic PET Radiochemistry Facility - 2015-08-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 3, 2015
- [FDA Inspection 886802 - Mayo Clinic PET Radiochemistry Facility - 2014-07-11](https://www.keypedia.com/records/fda_inspections/mayo-clinic-pet-radiochemistry-facility/f590a385-688d-48ba-9990-8cfdd7506c7a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 11, 2014
- FDA Inspection 771806 - Mayo Clinic PET Radiochemistry Facility - 2012-03-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 15, 2012

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