FDA Inspection 1316138 — Ankur Lodha, MD
The FDA completed an inspection of Ankur Lodha, MD on April 30, 2026 in Lafayette, LA. 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
- April 30, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Lafayette, LA (United States)
Additional Details
Clinical Investigator (CI)