# FDA Inspection 791521 - Mark Hoyer, M.D. - July 16, 2012

Source: https://www.keypedia.com/records/fda_inspections/mark-hoyer-md/5b4bd918-3af1-41ee-975d-d1a683b0ace9
Source feed: FDA_Inspections

> FDA Inspection 791521 for Mark Hoyer, M.D. on July 16, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791521
- Company Name: Mark Hoyer, M.D.
- Inspection Date: 2012-07-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/mark-hoyer-md/0cd534d1-4a44-4a4c-a809-e87391843970

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7