# FDA Inspection 1054438 - Bruce W. Bode, MD - May 04, 2018

Source: https://www.keypedia.com/records/fda_inspections/bruce-w-bode-md/40e3ac53-7a37-4efb-a197-69ff7bbea076
Source feed: FDA_Inspections

> FDA Inspection 1054438 for Bruce W. Bode, MD on May 04, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1054438
- Company Name: Bruce W. Bode, MD
- Inspection Date: 2018-05-04
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1200068 - 2023-03-09](https://www.keypedia.com/records/fda_inspections/bruce-w-bode-md/ca784005-7fce-49f7-8415-498322603ce8)
- [FDA Inspection 923452 - 2015-04-22](https://www.keypedia.com/records/fda_inspections/bruce-w-bode-md/ba50b529-a247-4012-996c-234718b68498)

Company: https://www.keypedia.com/companies/bruce-w-bode-md/68247dde-08c0-4139-9954-6dd43f9e597c

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