# FDA Inspection 773531 - Peter S. Hersh, M.D. - March 09, 2012

Source: https://www.keypedia.com/records/fda_inspections/peter-s-hersh-md/590898f5-a5af-4a9f-9a49-2e7639353fa6
Source feed: FDA_Inspections

> FDA Inspection 773531 for Peter S. Hersh, M.D. on March 09, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 773531
- Company Name: Peter S. Hersh, M.D.
- Inspection Date: 2012-03-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 864023 - 2014-01-16](https://www.keypedia.com/records/fda_inspections/peter-s-hersh-md/b9e88395-414c-4ed6-9084-048f6b4d1910)

Company: https://www.keypedia.com/companies/peter-s-hersh-md/7b55a971-b7b3-4fe9-80b1-d7218a5545be

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