# FDA Inspection 1195696 - David J. Goldberg, MD - January 11, 2023

Source: https://www.keypedia.com/records/fda_inspections/david-j-goldberg-md/04371cf1-bdcd-4385-ae6a-a37ea69db537
Source feed: FDA_Inspections

> FDA Inspection 1195696 for David J. Goldberg, MD on January 11, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195696
- Company Name: David J. Goldberg, MD
- Inspection Date: 2023-01-11
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 804866 - 2012-10-25](https://www.keypedia.com/records/fda_inspections/david-j-goldberg-md/b90eb255-58aa-4451-8182-e029114f0ac7)
- [FDA Inspection 778732 - 2012-04-27](https://www.keypedia.com/records/fda_inspections/david-j-goldberg-md/dae7f070-81ea-4acc-ac93-d56fa21588c1)

Company: https://www.keypedia.com/companies/david-j-goldberg-md/cf521521-d3ea-4381-811e-d7c9fb0634c3

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