FDA Inspection 1034135 — Dr. Zanete (NMI) Zvirbule

Dr. Zanete (NMI) Zvirbule — FEI 3013742549

The FDA completed an inspection of Dr. Zanete (NMI) Zvirbule on Nov 10, 2017 in Riga. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 10, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Riga (Latvia)

Additional Details

Clinical Investigator (CI)

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