FDA Inspection 1027091 — Darko Jovic

Darko Jovic — FEI 3013551661

The FDA completed an inspection of Darko Jovic on Aug 18, 2017 in Banja Luka, 78000. 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
Aug 18, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Banja Luka, 78000 (Bosnia-Hercegovina)

Additional details

Clinical Investigator (CI)

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