FDA Inspection
Rajendra R. Makkar, MDRajendra R. Makkar, MD – FDA Inspection, Aug 5, 2019
Record Details
This FDA Inspection record concerns Rajendra R. Makkar, MD, with an inspection on August 5, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · f2da2d38-16d7-4e55-8246-f3e998ad5a6c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1098769
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
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Other FDA inspections of Rajendra R. Makkar, MD
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 15, 2023 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| July 28, 2023 | Not classified | Los Angeles District Office | |
| April 15, 2016 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| December 14, 2012 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Rajendra R. Makkar, MD
- FDA Inspection 1215918 - 2023-08-15
- FDA Inspection 1214834 - 2023-07-28
- FDA Inspection 974214 - 2016-04-15
- FDA Inspection 810604 - 2012-12-14
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