# FDA 483 - Suneet Mittal, MD - July 11, 2023

Source: https://www.keypedia.com/records/483/suneet-mittal-md/cc7515ec-b205-4b78-a1f4-7db550e5cf7a

> FDA 483 for Suneet Mittal, MD on July 11, 2023. Product: drugs. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: Suneet Mittal, MD
- Inspection Date: 2023-07-11
- Product Type: drugs
- Office Name: New Jersey District Office
- Summary: Suneet Mittal, MD in Paramus, NJ, a clinical investigator, was issued a Form FDA 483 following an inspection from June 21 to July 11, 2023. The inspection revealed that an investigation was not conducted according to the investigational plan, specifically concerning the handling and timely evaluation of 22 retrospectively identified adverse events. This indicates a significant lapse in clinical trial oversight and patient safety protocols.

## Related Officers

- [investigator](https://www.keypedia.com/people/tyanna-n-hadley/8fdebfd7-d6f3-44ab-9dcb-864ab6d55d53)

Company: https://www.keypedia.com/companies/suneet-mittal-md/ffb11dda-99f9-435a-b51b-feb9c3bcc144

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