# FDA Inspection 920224 - Demetrius K. Lopes, M.D. - June 25, 2015

Source: https://www.keypedia.com/records/fda_inspections/demetrius-k-lopes-md/a0abd735-27af-4bc9-9568-528510278724
Source feed: FDA_Inspections

> FDA Inspection 920224 for Demetrius K. Lopes, M.D. on June 25, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 920224
- Company Name: Demetrius K. Lopes, M.D.
- Inspection Date: 2015-06-25
- Classification: Official Action Indicated (OAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1225756 - 2023-12-11](https://www.keypedia.com/records/fda_inspections/demetrius-k-lopes-md/b0fce4d7-a7cf-4272-b3a8-85a17f9ed68b)

Company: https://www.keypedia.com/companies/demetrius-k-lopes-md/7f37f8f0-5b27-4ee7-9972-4f6435f169bd

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