# FDA 483 - Dennis Hammond - June 20, 2023

Source: https://www.keypedia.com/records/483/dennis-hammond/4a4bdd4d-aa62-41e4-bda5-5bb0b7b69224

> FDA 483 for Dennis Hammond on June 20, 2023. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Dennis Hammond
- Inspection Date: 2023-06-20
- Product Type: other
- Office Name: Division of Pharmaceutical Quality Operations III
- Summary: Dennis Hammond, a clinical investigator in Grand Rapids, MI, was inspected by the FDA from June 12-20, 2023. The inspection revealed that investigations were not conducted in accordance with agreements and regulations, specifically regarding the timely reporting of serious adverse events. Additionally, required records, such as adverse event forms, were not consistently completed and maintained in subject records.

## Related Officers

- [issuing_officer](https://www.keypedia.com/people/jennifer-a-kemp/51aa8f2f-ba64-47d3-aa06-b4595b3d15c8)
- [investigator](https://www.keypedia.com/people/chelsea-w-lamm/d7a8dd67-dc26-4c8a-8e3c-aebc267cb775)

Company: https://www.keypedia.com/companies/dennis-hammond/e48f0e6c-487e-49f7-b87a-b51e616a2710

Office: https://www.keypedia.com/offices/division-of-pharmaceutical-quality-operations-iii/45bc2d0d-d731-4955-aeb5-59aa0b76e4f0