# Suzanne Bruce, M.D. – FDA Inspection, Aug 3, 2012

Source: https://www.keypedia.com/records/fda_inspections/suzanne-bruce-md/88290129-bd9a-4293-b3da-eadb769f4077
Source feed: FDA_Inspections

> FDA inspection 794721 of Suzanne Bruce, M.D., August 03, 2012. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 812. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 794721
- Company Name: Suzanne Bruce, M.D.
- Inspection Date: 2012-08-03
- 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: 3

## Related Documents

- FDA Inspection 1124193 - 2020-06-11
- FDA Inspection 744842 - 2011-08-23
- FDA Inspection 598996 - 2009-07-17
- FDA Inspection 571172 - 2009-03-19

Company: https://www.keypedia.com/companies/suzanne-bruce-md/09249bfb-bd19-41ba-b9c4-0bc49f0c142d

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