FDA Inspection 999629 — Salomon Stemmer
The FDA completed an inspection of Salomon Stemmer on Feb 2, 2017 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 2, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Petach Tikva (Israel)
Additional Details
Clinical Investigator (CI)