# Bruce G. Goldner, MD – FDA Inspection, Jan 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/bruce-g-goldner-md/f0ce3544-149d-49b8-b49a-b7386d471552
Source feed: FDA_Inspections

> FDA inspection 955851 of Bruce G. Goldner, MD, January 22, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 312. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 955851
- Company Name: Bruce G. Goldner, MD
- Inspection Date: 2016-01-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1228370 - 2024-01-24

Company: https://www.keypedia.com/companies/bruce-g-goldner-md/5a08efd9-1c44-4a13-9de2-a4db5dc67e03

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