FDA Inspection 632101 — Mederi Therapeutics, Inc

Mederi Therapeutics, Inc — FEI 3007729452

The FDA completed an inspection of Mederi Therapeutics, Inc on Dec 3, 2009 in Norwalk, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 3, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Norwalk, CT (United States)