FDA Inspection 1039234 — Hyo Jong Kim

Hyo Jong Kim — FEI 3013664405

The FDA completed an inspection of Hyo Jong Kim on Oct 26, 2017 in Seoul. 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
Oct 26, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Seoul (Korea (the Republic of))

Additional details

Clinical Investigator (CI)

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