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FDA Inspection
•Suneet Mittal, MD•July 11, 2023

Suneet Mittal, MD – FDA Inspection, Jul 11, 2023

Record Details

This FDA Inspection record concerns Suneet Mittal, MD, with an inspection on July 11, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Suneet Mittal, MD
Inspection Date
July 11, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Tyanna N. Hadley (Company Rep)
View Company Profile

ID · 1fa8d294-689f-4f9f-b1e0-e71763750fb4

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1209805
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
  2. 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Suneet Mittal, MD

2
DateClassificationOfficeProject area
August 23, 2018NAICenter for Devices and Radiological HealthBioresearch Monitoring
June 5, 2014VAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Suneet Mittal, MD
  • FDA Inspection 1065642 - 2018-08-23
  • FDA Inspection 875338 - 2014-06-05

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