Atul Verma – FDA Inspection, Aug 11, 2023

Record Details

This FDA Inspection record concerns Atul Verma, with an inspection on August 11, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: Atul Verma
Inspection Date: August 11, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Stuart W. Russell (FDA Associated Person)

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ID · aa4e20eb-b540-481c-ac25-b181b13982f3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number: 1215414
FDA center: Medical Devices & Rad Health
Project area: Bioresearch Monitoring
Outcome: Form 483 issued, view the record

FDA Citations

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

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FDA Inspection

Atul VermaAugust 11, 2023