FDA Inspection 1062461 — Synexus - Chandler

Synexus - Chandler — FEI 3009767607

The FDA completed an inspection of Synexus - Chandler on Jul 20, 2018 in Chandler, AZ. 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
Jul 20, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chandler, AZ (United States)

Additional Details

Clinical BA/BE