Rishi K. Wadhwa, M.D. – FDA Inspection, Mar 20, 2026

Record Details

This FDA Inspection record concerns Rishi K. Wadhwa, M.D., with an inspection on March 20, 2026, issued by the New Orleans District Office, covering medical devices & rad health.

Company: Rishi K. Wadhwa, M.D.
Inspection Date: March 20, 2026
Product Type: Medical Devices & Rad Health
Office: New Orleans District Office
Person: Theressa B. Smith (Issuing Officer)

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ID · 9dbbd3d0-6740-45df-ae51-225ec19ee1fa

Inspection Facts

Inspection number: 1308694
FDA center: Medical Devices & Rad Health
Project area: Product Evaluation: Medical Devices
Outcome: Form 483 issued, view the record

FDA Citations

21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
21 CFR 812.140(a)(3)(ii)Investigator records of relevant observations inadequate

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FDA Inspection

Rishi K. Wadhwa, M.D.March 20, 2026