# FDA Inspection 718966 - Gregory A. Hoffman, M.D. - March 25, 2011

Source: https://www.keypedia.com/records/fda_inspections/gregory-a-hoffman-md/7ed55f4a-fb8c-4034-a936-1a0cf9ed2fc8
Source feed: FDA_Inspections

> FDA Inspection 718966 for Gregory A. Hoffman, M.D. on March 25, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 718966
- Company Name: Gregory A. Hoffman, M.D.
- Inspection Date: 2011-03-25
- 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/gregory-a-hoffman-md/b0f51fcb-4b9e-4741-b608-4cbb58346ffa

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