Aarti K. Bhatia, MD, MPH – FDA Inspection, Aug 7, 2026

Record Details

This FDA Inspection record concerns Aarti K. Bhatia, MD, MPH, with an inspection on August 7, 2026, issued by the New England District Office, covering human drugs.

Company: Aarti K. Bhatia, MD, MPH
Inspection Date: August 7, 2026
Product Type: Human Drugs
Office: New England District Office
Person: Jose A. Torres (Company Rep)

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ID · cf2852b5-1760-45b1-a47c-1d16335d9860

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number: 1329870
FDA center: Human Drugs
Project area: Bioresearch Monitoring
Outcome: Form 483 issued, view the record

FDA Citations

21 CFR 50.20Consent not obtained, exceptions do not apply

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FDA Inspection

Aarti K. Bhatia, MD, MPHAugust 7, 2026