# FDA 483 - Atul Verma - August 11, 2023

Source: https://www.keypedia.com/records/483/atul-verma/ae75e9dc-4c9a-47c0-afbe-6917693c7beb

> FDA 483 for Atul Verma on August 11, 2023. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Atul Verma
- Inspection Date: 2023-08-11
- Product Type: other
- Office Name: Center for Devices and Radiological Health
- Summary: An FDA inspection of clinical investigator Atul Verma, M.D. identified a significant issue regarding the conduct of a clinical study. The firm failed to follow good clinical practice for record accuracy, specifically noting discrepancies between source documentation and the electronic database for the Medtronic MDT 16027 clinical study. This indicates a failure to properly investigate and maintain accurate records for patient data.

## Related Officers

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

Company: https://www.keypedia.com/companies/atul-verma/e80ee3ce-e137-47bf-a5ef-d076a733f76a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7