# FDA Inspection 589023 - Goldman, Mitchel P MD - June 12, 2009

Source: https://www.keypedia.com/records/fda_inspections/goldman-mitchel-p-md/f3cb53f8-06a1-45e1-abf6-bd3eb50ee1d0
Source feed: FDA_Inspections

> FDA Inspection 589023 for Goldman, Mitchel P MD on June 12, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 589023
- Company Name: Goldman, Mitchel P MD
- Inspection Date: 2009-06-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 796672 - 2012-08-24](https://www.keypedia.com/records/fda_inspections/goldman-mitchel-p-md/74c048ae-c1b9-46a7-bb34-5d476af0f5d0)

Company: https://www.keypedia.com/companies/goldman-mitchel-p-md/72678d7e-7a87-4e05-a1bf-60aafeddf53b

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