FDA Inspection 918004 — Embera NeuroTherapeutics, Inc

Embera NeuroTherapeutics, Inc — FEI 3011410181

The FDA completed an inspection of Embera NeuroTherapeutics, Inc on Mar 18, 2015 in Shreveport, LA. 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
Mar 18, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Shreveport, LA (United States)

Additional Details

Sponsor, Contract Research Organization