# FDA Inspection 840881 - Peter Helton M.D. - July 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/peter-helton-md/b9670826-cc7e-4694-8e3c-5f10be6cf35c
Source feed: FDA_Inspections

> FDA Inspection 840881 for Peter Helton M.D. on July 12, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 840881
- Company Name: Peter Helton M.D.
- Inspection Date: 2013-07-12
- 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/peter-helton-md/616ab30a-24e2-4f62-b0d0-ae02688dca7a

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