# Andrew R. Gould, M.D. – FDA Inspection, Aug 8, 2019

Source: https://www.keypedia.com/records/fda_inspections/andrew-r-gould-md/7484d94c-f2aa-4d5e-88bf-84feb9642cbf
Source feed: FDA_Inspections

> FDA inspection 1099007 of Andrew R. Gould, M.D., August 08, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099007
- Company Name: Andrew R. Gould, M.D.
- Inspection Date: 2019-08-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1016474 - 2017-06-19

## Related Officers

- [Company Rep](https://www.keypedia.com/people/karen-m-cooper/4813e60d-c8da-4df2-bc48-ecfb06a55cf8)

Company: https://www.keypedia.com/companies/andrew-r-gould-md/73bc1e8e-a58f-4361-aa90-48620ea4f6c9

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