# FDA 483 - E. Jeffrey Greenberg, MD - May 30, 2018

Source: https://www.globalkeysolutions.net/records/483/e-jeffrey-greenberg-md/17a80789-65ed-4b50-b040-52bba0936706

> FDA 483 for E. Jeffrey Greenberg, MD on May 30, 2018. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: E. Jeffrey Greenberg, MD
- Inspection Date: 2018-05-30
- Product Type: drugs
- Office Name: New Jersey District Office
- Summary: An FDA inspection of E. Jeffrey Greenberg, MD, a clinical investigator in Somerset, NJ, revealed two significant observations. The firm failed to conduct an investigation in accordance with its investigational plan, specifically regarding incorrect scoring of a test for study subjects. Additionally, the firm did not maintain adequate case histories, as multiple study notes for several subjects were not signed or dated by the individuals conducting the procedures.

## Related Officers

- [Regulatory Officer](https://www.globalkeysolutions.net/people/peter-r-lenahan/c695dac2-5447-434b-801e-f95e6acf05f1)

Company: https://www.globalkeysolutions.net/companies/e-jeffrey-greenberg-md/9b48dfe4-b63b-41ca-89ff-f6cc2c79b5cb

Office: https://www.globalkeysolutions.net/offices/new-jersey-district-office/6ff5e2e9-5cff-44c7-af24-5a55329a8248