# Rajendra R. Makkar, MD – FDA Inspection, Aug 5, 2019

Source: https://www.keypedia.com/records/fda_inspections/rajendra-r-makkar-md/f2da2d38-16d7-4e55-8246-f3e998ad5a6c
Source feed: FDA_Inspections

> FDA inspection 1098769 of Rajendra R. Makkar, MD, August 05, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1098769
- Company Name: Rajendra R. Makkar, MD
- Inspection Date: 2019-08-05
- 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: 1

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- [FDA Inspection 810604 - 2012-12-14](https://www.keypedia.com/records/fda_inspections/rajendra-r-makkar-md/0e104e83-f213-42c2-94be-aa6c92f7afe0)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/angela-shepas/743113c1-799b-44e9-9422-8049c476bfd2)

Company: https://www.keypedia.com/companies/rajendra-r-makkar-md/9bc82c8e-f40e-416b-af12-93d21d5cf458

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