# Goodman, Roger D.D.S. – FDA Inspection, Jun 9, 2015

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

> FDA inspection 929512 of Goodman, Roger D.D.S., June 09, 2015. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 797869 - 2012-09-04
- FDA Inspection 682781 - 2010-10-08

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