FDA Inspection 1277788 — Haresh D. Boghara, MD

Haresh D. Boghara, MD — FEI 3038237143

The FDA completed an inspection of Haresh D. Boghara, MD on August 1, 2025 in Desoto, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 1, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Desoto, TX (United States)

Additional Details

Clinical Investigator (CI)