# FDA 483 - Robert D. Ferrera, MD - May 22, 2008

Source: https://www.globalkeysolutions.net/records/483/robert-d-ferrera-md/71e9d228-de61-4196-bf9e-08826cc8d11e

> FDA 483 for Robert D. Ferrera, MD on May 22, 2008. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Robert D. Ferrera, MD
- Inspection Date: 2008-05-22
- Product Type: drugs
- Office Name: Division of Human and Animal Food Operations - West V
- Summary: An FDA inspection of Ferrera, R. David, MD in Sacramento, CA, a clinical investigator, revealed significant issues with the conduct of a clinical investigation. The firm failed to follow the signed statement of investigator, specifically regarding incorrect drug kit dispensation and the failure to report an adverse event for a study subject. These observations indicate a lack of adherence to proper clinical trial procedures.

## Related Officers

- [Stuart W. Russell](https://www.globalkeysolutions.net/people/stuart-w-russell/59719ee0-e7b3-4e10-8d87-7c79eb2c2192)

Company: https://www.globalkeysolutions.net/companies/robert-d-ferrera-md/63b28019-2fc7-45e3-8a77-eb33b48faf5b

Office: https://www.globalkeysolutions.net/offices/division-of-human-and-animal-food-operations-west-v/0f4dd01e-8e8a-4336-9abe-ce8b3d309e8b