# Robert A. Weiss, M.D. – FDA Inspection, Oct 29, 2019

Source: https://www.keypedia.com/records/fda_inspections/robert-a-weiss-md/35b047f3-4f90-49a0-842f-0dd346436397
Source feed: FDA_Inspections

> FDA inspection 1107837 of Robert A. Weiss, M.D., October 29, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 312. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1107837
- Company Name: Robert A. Weiss, M.D.
- Inspection Date: 2019-10-29
- 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: 1

## Related Documents

- FDA Inspection 1206481 - 2023-05-19
- FDA Inspection 947315 - 2015-10-27
- FDA Inspection 846083 - 2013-08-26

Company: https://www.keypedia.com/companies/robert-a-weiss-md/19f2b2e4-401d-4d04-8a9b-0fe0f9569d8b

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