# FDA Inspection 1176020 - Kenneth J. Rosenthal, M.D. - June 29, 2022

Source: https://www.keypedia.com/records/fda_inspections/kenneth-j-rosenthal-md/ca2e96ec-4a2b-4d5f-a4b3-2c622228a995
Source feed: FDA_Inspections

> FDA Inspection 1176020 for Kenneth J. Rosenthal, M.D. on June 29, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1176020
- Company Name: Kenneth J. Rosenthal, M.D.
- Inspection Date: 2022-06-29
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 982365 - 2016-08-11](https://www.keypedia.com/records/fda_inspections/kenneth-j-rosenthal-md/a07774a9-3530-46f9-9a84-a07db51e769b)
- [FDA Inspection 646264 - 2010-01-27](https://www.keypedia.com/records/fda_inspections/kenneth-j-rosenthal-md/3b30556a-0626-42df-becf-52962b2115df)

Company: https://www.keypedia.com/companies/kenneth-j-rosenthal-md/337a8ad7-284e-4cae-8ba8-a09329cd46a2

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