FDA Inspection 1083162 — Salomon Stemmer

Salomon Stemmer — FEI 3012769888

The FDA completed an inspection of Salomon Stemmer on Feb 26, 2019 in Petach Tikva. 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
Feb 26, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Petach Tikva (Israel)

Additional Details

Clinical Investigator (CI)

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