# FDA 483 - Amer M. Zeidan, M.D. - August 08, 2025

Source: https://www.globalkeysolutions.net/records/483/amer-m-zeidan-md/cdffb567-d1a7-48fd-b5e6-47692983c75d

> FDA 483 for Amer M. Zeidan, M.D. on August 08, 2025. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Amer M. Zeidan, M.D.
- Inspection Date: 2025-08-08
- Product Type: drugs
- Office Name: New England District Office
- Summary: Amer M. Zeidan, M.D. in New Haven, CT, a clinical investigator, was issued a Form FDA 483 following an inspection. The inspection revealed a failure to maintain accurate case histories for a clinical study. Specifically, data points from bone marrow pathology reports were incorrectly entered into the electronic data capture system.

## Related Officers

- [Darin S. Wiegers](https://www.globalkeysolutions.net/people/darin-s-wiegers/5bf03f8b-1571-4845-916d-3211d72d97a2)
- [issuing_officer](https://www.globalkeysolutions.net/people/kent-a-conforti/8d3d3e82-cd97-420e-8840-df92d6eeba09)

Company: https://www.globalkeysolutions.net/companies/amer-m-zeidan-md/12531e1e-e9ea-4f1c-9311-4da2596a2f89

Office: https://www.globalkeysolutions.net/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144