# Atul Verma – FDA Inspection, Aug 11, 2023

Source: https://www.keypedia.com/records/fda_inspections/atul-verma/aa4e20eb-b540-481c-ac25-b181b13982f3
Source feed: FDA_Inspections

> FDA inspection 1215414 of Atul Verma, August 11, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1215414
- Company Name: Atul Verma
- Inspection Date: 2023-08-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [FDA Associated Person](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