# FDA Inspection 1217141 - John D. Hummel, M.D. - August 25, 2023

Source: https://www.keypedia.com/records/fda_inspections/john-d-hummel-md/9b1a451e-dc9b-471b-9117-fa78a89cdfb7
Source feed: FDA_Inspections

> FDA Inspection 1217141 for John D. Hummel, M.D. on August 25, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1217141
- Company Name: John D. Hummel, M.D.
- Inspection Date: 2023-08-25
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 663983 - 2010-06-11](https://www.keypedia.com/records/fda_inspections/john-d-hummel-md/bbd92269-06d1-47f0-abfe-eae750a8f82a)

Company: https://www.keypedia.com/companies/john-d-hummel-md/faade96c-6b53-414c-b7bd-ecaa3263be10

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