# FDA Inspection 929512 - Goodman, Roger D.D.S. - June 09, 2015

Source: https://www.keypedia.com/records/fda_inspections/goodman-roger-dds/63b33ba1-2cb3-4d3b-8643-a90681de7d24
Source feed: FDA_Inspections

> FDA Inspection 929512 for Goodman, Roger D.D.S. on June 09, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 929512
- Company Name: Goodman, Roger D.D.S.
- Inspection Date: 2015-06-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/goodman-roger-dds/42a3421c-eda9-4328-b8bb-e5d64d469a45

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