# FDA Inspection 862345 - Barry D Bertolet, MD - December 06, 2013

Source: https://www.keypedia.com/records/fda_inspections/barry-d-bertolet-md/6c81ed91-acb5-4a71-b33b-ce0ffe592d83
Source feed: FDA_Inspections

> FDA Inspection 862345 for Barry D Bertolet, MD on December 06, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 862345
- Company Name: Barry D Bertolet, MD
- Inspection Date: 2013-12-06
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1144718 - 2021-06-11](https://www.keypedia.com/records/fda_inspections/barry-d-bertolet-md/4faf0bf7-02aa-49c3-b706-f5516ab88de8)

Company: https://www.keypedia.com/companies/barry-d-bertolet-md/ea6cf532-48d5-4c17-ac1d-6f8c14d7b19a

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