# FDA Inspection 839676 - Kenneth A. Pettine, MD - June 28, 2013

Source: https://www.keypedia.com/records/fda_inspections/kenneth-a-pettine-md/60c0d978-b665-4f28-8abe-86e661fd0010
Source feed: FDA_Inspections

> FDA Inspection 839676 for Kenneth A. Pettine, MD on June 28, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 839676
- Company Name: Kenneth A. Pettine, MD
- Inspection Date: 2013-06-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 581731 - 2009-03-30](https://www.keypedia.com/records/fda_inspections/kenneth-a-pettine-md/ac68de45-5836-4fa6-a880-58f1700f88ef)

Company: https://www.keypedia.com/companies/kenneth-a-pettine-md/3bed1283-ce0f-41a1-abf8-37fac67edfa2

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