FDA Inspection 1083313 — Diana-Hortensia Barbonta, MD

Diana-Hortensia Barbonta, MD — FEI 3014930991

The FDA completed an inspection of Diana-Hortensia Barbonta, MD on Mar 1, 2019 in Alba Iulia. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 1, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Alba Iulia (Romania)

Additional Details

Clinical Investigator (CI)

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