FDA Inspection 1030676 — Parita Bhuva, MD

Parita Bhuva, MD — FEI 3013784407

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)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.