FDA Inspection 1030676 — Parita Bhuva, MD
The FDA completed an inspection of Parita Bhuva, MD on Oct 18, 2017 in Plano, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Oct 18, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Plano, TX (United States)
Additional details
Clinical Investigator (CI)