# Paul Sorajja, M.D., Clinical Investigator – FDA Inspection, Mar 22, 2019

Source: https://www.keypedia.com/records/fda_inspections/paul-sorajja-md-clinical-investigator/4889b481-2be8-47f4-a99b-c4590cffcadc
Source feed: FDA_Inspections

> FDA inspection 1083532 of Paul Sorajja, M.D., Clinical Investigator, March 22, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 50 and 812. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1083532
- Company Name: Paul Sorajja, M.D., Clinical Investigator
- Inspection Date: 2019-03-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1269127 - 2025-05-02
- [FDA Inspection 1215907 - 2023-08-25](https://www.keypedia.com/records/fda_inspections/paul-sorajja-md-clinical-investigator/5eca3c30-5a14-41a0-81d4-3ab51afd79df)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/kellie-l-thommes/255a1b92-cd56-41f5-9622-82e8a629e153)

Company: https://www.keypedia.com/companies/paul-sorajja-md-clinical-investigator/3122779d-6e12-46e7-a5b3-609479cb3205

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