FDA Inspection 1037322 — Maria Turdean

Maria Turdean — FEI 3013844657

The FDA completed an inspection of Maria Turdean on Dec 8, 2017 in Cluj, 400006. 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
Dec 8, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cluj, 400006 (Romania)

Additional Details

Clinical Investigator (CI)

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