FDA Inspection 1039081 — Shani Paluch-Shimon

Shani Paluch-Shimon — FEI 3013828608

The FDA completed an inspection of Shani Paluch-Shimon on Dec 12, 2017 in Jerusalem. 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 12, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Jerusalem (Israel)

Additional details

Clinical Investigator (CI)

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